Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502794_38502804delinsGGGGCAGGGGC , CM000681.2:g.38502794_38502804delinsGGGGCAGGGGC	GRCh38
NC_000019.9:g.38993434_38993444delinsGGGGCAGGGGC , CM000681.1:g.38993434_38993444delinsGGGGCAGGGGC	GRCh37
NC_000019.8:g.43685274_43685284delinsGGGGCAGGGGC	NCBI36
NG_008866.1:g.74095_74105delinsGGGGCAGGGGC , LRG_766:g.74095_74105delinsGGGGCAGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7835+67_7836-76delinsGGGGCAGGGGC	ENSP00000471601.2:n.7835+67_7836-76delinsGGGGCAGGGGC
ENST00000359596.8:c.7835+67_7836-76delinsGGGGCAGGGGC MANE Select	ENSP00000352608.2:n.7835+67_7836-76delinsGGGGCAGGGGC
ENST00000355481.8:c.7835+67_7836-76delinsGGGGCAGGGGC	ENSP00000347667.3:n.7835+67_7836-76delinsGGGGCAGGGGC
ENST00000359596.7:c.7835+67_7836-76delinsGGGGCAGGGGC	ENSP00000352608.2:n.7835+67_7836-76delinsGGGGCAGGGGC
ENST00000360985.7:c.7832+67_7833-76delinsGGGGCAGGGGC	ENSP00000354254.4:n.7832+67_7833-76delinsGGGGCAGGGGC
ENST00000594335.5:c.1287+67_1288-76delinsGGGGCAGGGGC
NM_000540.2:c.7835+67_7836-76delinsGGGGCAGGGGC , LRG_766t1:c.7835+67_7836-76delinsGGGGCAGGGGC	NP_000531.2:n.7835+67_7836-76delinsGGGGCAGGGGC
NM_001042723.1:c.7835+67_7836-76delinsGGGGCAGGGGC	NP_001036188.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_006723317.1:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_006723380.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_006723319.1:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_006723382.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_011527204.1:c.7832+67_7833-76delinsGGGGCAGGGGC	XP_011525506.1:n.7832+67_7833-76delinsGGGGCAGGGGC
XM_011527205.1:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_011525507.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_006723317.2:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_006723380.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_006723319.2:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_006723382.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XM_011527205.2:c.7835+67_7836-76delinsGGGGCAGGGGC	XP_011525507.1:n.7835+67_7836-76delinsGGGGCAGGGGC
XR_001753735.1:n.7918+67_7919-76delinsGGGGCAGGGGC
NM_000540.3:c.7835+67_7836-76delinsGGGGCAGGGGC MANE Select	NP_000531.2:n.7835+67_7836-76delinsGGGGCAGGGGC
NM_001042723.2:c.7835+67_7836-76delinsGGGGCAGGGGC	NP_001036188.1:n.7835+67_7836-76delinsGGGGCAGGGGC