Canonical Allele Identifier: CA136866772
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271153_31271154delinsC , CM000668.2:g.31271153_31271154delinsC GRCh38
NC_000006.11:g.31238930_31238931delinsC , CM000668.1:g.31238930_31238931delinsC GRCh37
NC_000006.10:g.31346909_31346910delinsC NCBI36
NG_029422.2:g.5978_5979delinsG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.538_539delinsG MANE Select ENSP00000365402.5:p.Leu180GlyfsTer?
ENST00000376228.9:c.538_539delinsG ENSP00000365402.5:p.Leu180GlyfsTer?
ENST00000376237.8:c.*125_*126delinsG ENSP00000365412.4:n.*125_*126delinsG
ENST00000383329.7:c.538_539delinsG ENSP00000372819.3:p.Leu180GlyfsTer?
ENST00000415537.1:c.536_537delinsG
ENST00000484378.1:n.807_808delinsG
ENST00000487245.5:n.897_898delinsG
ENST00000495835.1:n.727_728delinsG
NM_002117.5:c.538_539delinsG NP_002108.4:p.Leu180GlyfsTer?
NM_002117.6:c.538_539delinsG MANE Select NP_002108.4:p.Leu180GlyfsTer?