Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38499445_38499490delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA , CM000681.2:g.38499445_38499490delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	GRCh38
NC_000019.9:g.38990085_38990130delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA , CM000681.1:g.38990085_38990130delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	GRCh37
NC_000019.8:g.43681925_43681970delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	NCBI36
NG_008866.1:g.70746_70791delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA , LRG_766:g.70746_70791delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	ENSP00000471601.2:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCC...
ENST00000359596.8:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA MANE Select	ENSP00000352608.2:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCC...
ENST00000355481.8:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	ENSP00000347667.3:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCC...
ENST00000359596.7:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	ENSP00000352608.2:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCC...
ENST00000360985.7:c.7025-190_7025-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	ENSP00000354254.4:n.7025-190_7025-145delinsGGGAGCCTGGTGTTACCC...
ENST00000594335.5:c.480-190_480-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA
NM_000540.2:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA , LRG_766t1:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	NP_000531.2:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAG...
NM_001042723.1:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	NP_001036188.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_006723317.1:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_006723380.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_006723319.1:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_006723382.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_011527204.1:c.7025-190_7025-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_011525506.1:n.7025-190_7025-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_011527205.1:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_011525507.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_006723317.2:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_006723380.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_006723319.2:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_006723382.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XM_011527205.2:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	XP_011525507.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...
XR_001753735.1:n.7111-190_7111-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA
NM_000540.3:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA MANE Select	NP_000531.2:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAG...
NM_001042723.2:c.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTAGAGGTGTTGGGTCCTGGGGCTGGCA	NP_001036188.1:n.7028-190_7028-145delinsGGGAGCCTGGTGTTACCCCTA...