Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102840315_102840316insAGGGTAGATTTTGGTTTGGTTTATTTGGACATGATATCCAAATCTCGCAAGTAGAACCATTGCGGCTCAATATTGTAAATTCTAAATCAGTATCTTCTTTGTCTATAAATTTA , CM000674.2:g.102840315_102840316insAGGGTAGATTTTGGTTTGGTTTATTTGGACATGATATCCAAATCTCGCAAGTAGAACCATTGCGGCTCAATATTGTAAATTCTAAATCAGTATCTTCTTTGTCTATAAATTTA	GRCh38
NC_000012.11:g.103234093_103234094insAGGGTAGATTTTGGTTTGGTTTATTTGGACATGATATCCAAATCTCGCAAGTAGAACCATTGCGGCTCAATATTGTAAATTCTAAATCAGTATCTTCTTTGTCTATAAATTTA , CM000674.1:g.103234093_103234094insAGGGTAGATTTTGGTTTGGTTTATTTGGACATGATATCCAAATCTCGCAAGTAGAACCATTGCGGCTCAATATTGTAAATTCTAAATCAGTATCTTCTTTGTCTATAAATTTA	GRCh37
NC_000012.10:g.101758223_101758224insAGGGTAGATTTTGGTTTGGTTTATTTGGACATGATATCCAAATCTCGCAAGTAGAACCATTGCGGCTCAATATTGTAAATTCTAAATCAGTATCTTCTTTGTCTATAAATTTA	NCBI36
NG_008690.1:g.82296_82297insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT
NG_008690.2:g.123104_123105insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT MANE Select	ENSP00000448059.1:n.1315+93_1315+94insAGA...
ENST00000307000.7:c.1300+93_1300+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	ENSP00000303500.2:n.1300+93_1300+94insAGA...
ENST00000551114.2:n.977+93_977+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT
ENST00000553106.5:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	ENSP00000448059.1:n.1315+93_1315+94insAGA...
ENST00000635477.1:c.419+93_419+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT
ENST00000635528.1:n.830+93_830+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT
NM_000277.1:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	NP_000268.1:n.1315+93_1315+94insAGACAAAGA...
XM_011538422.1:c.1258+93_1258+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	XP_011536724.1:n.1258+93_1258+94insAGACAA...
NM_000277.2:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	NP_000268.1:n.1315+93_1315+94insAGACAAAGA...
NM_001354304.1:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	NP_001341233.1:n.1315+93_1315+94insAGACAA...
NM_000277.3:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT MANE Select	NP_000268.1:n.1315+93_1315+94insAGACAAAGA...
NM_001354304.2:c.1315+93_1315+94insAGACAAAGAAGATACTGATTTAGAATTTACAATATTGAGCCGCAATGGTTCTACTTGCGAGATTTGGATATCATGTCCAAATAAACCAAACCAAAATCTACCCTTAAATTTAT	NP_001341233.1:n.1315+93_1315+94insAGACAA...