Canonical Allele Identifier: CA1619080691
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271551G= , CM000668.2:g.31271551G= GRCh38
NC_000006.11:g.31239328G= , CM000668.1:g.31239328G= GRCh37
NC_000006.10:g.31347307G= NCBI36
NG_029422.2:g.5581C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+48C= MANE Select ENSP00000365402.5:n.343+48C=
ENST00000376228.9:c.343+48C= ENSP00000365402.5:n.343+48C=
ENST00000376237.8:c.343+48C= ENSP00000365412.4:n.343+48C=
ENST00000383329.7:c.343+48C= ENSP00000372819.3:n.343+48C=
ENST00000415537.1:c.341+48C=
ENST00000484378.1:n.410C=
ENST00000487245.5:n.500C=
ENST00000495835.1:n.532+48C=
NM_002117.5:c.343+48C= NP_002108.4:n.343+48C=
NM_002117.6:c.343+48C= MANE Select NP_002108.4:n.343+48C=