Canonical Allele Identifier: CA2844096461
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271238_31271239dup , CM000668.2:g.31271238_31271239dup GRCh38
NC_000006.11:g.31239015_31239016dup , CM000668.1:g.31239015_31239016dup GRCh37
NC_000006.10:g.31346994_31346995dup NCBI36
NG_029422.2:g.5893_5894dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.453_454dup MANE Select ENSP00000365402.5:p.Glu152AlafsTer30
ENST00000376228.9:c.453_454dup ENSP00000365402.5:p.Glu152AlafsTer30
ENST00000376237.8:c.*40_*41dup ENSP00000365412.4:n.*40_*41dup
ENST00000383329.7:c.453_454dup ENSP00000372819.3:p.Glu152AlafsTer30
ENST00000415537.1:c.451_452dup
ENST00000484378.1:n.722_723dup
ENST00000487245.5:n.812_813dup
ENST00000495835.1:n.642_643dup
NM_002117.5:c.453_454dup NP_002108.4:p.Glu152AlafsTer30
NM_002117.6:c.453_454dup MANE Select NP_002108.4:p.Glu152AlafsTer30