Canonical Allele Identifier: CA1619078484
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761153529

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269860_31269861insAT , CM000668.2:g.31269860_31269861insAT GRCh38
NC_000006.11:g.31237637_31237638insAT , CM000668.1:g.31237637_31237638insAT GRCh37
NC_000006.10:g.31345616_31345617insAT NCBI36
NG_029422.2:g.7271_7272insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+105_1015+106insAT MANE Select ENSP00000365402.5:n.1015+105_1015+106insA...
ENST00000376228.9:c.1015+105_1015+106insAT ENSP00000365402.5:n.1015+105_1015+106insA...
ENST00000376237.8:c.*602+105_*602+106insAT ENSP00000365412.4:n.*602+105_*602+106insA...
ENST00000383329.7:c.1015+105_1015+106insAT ENSP00000372819.3:n.1015+105_1015+106insA...
ENST00000470363.5:n.438_439insAT
ENST00000487245.5:n.1374+105_1374+106insAT
NM_002117.5:c.1015+105_1015+106insAT NP_002108.4:n.1015+105_1015+106insAT
NM_002117.6:c.1015+105_1015+106insAT MANE Select NP_002108.4:n.1015+105_1015+106insAT