Canonical Allele Identifier: CA3710434

Gene: HLA-C

Linked Data

• dbSNP Id: rs751406601
• ExAC: 6:31237960 G / GC
• gnomAD v4: 6-31270183-G-GC
• MyVariant Identifiers: chr6:g.31237960_31237961insC (hg19) ; chr6:g.31270183_31270184insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270183_31270184insC , CM000668.2:g.31270183_31270184insC	GRCh38
NC_000006.11:g.31237960_31237961insC , CM000668.1:g.31237960_31237961insC	GRCh37
NC_000006.10:g.31345939_31345940insC	NCBI36
NG_029422.2:g.6948_6949insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+26_895+27insG MANE Select	ENSP00000365402.5:n.895+26_895+27insG
ENST00000376228.9:c.895+26_895+27insG	ENSP00000365402.5:n.895+26_895+27insG
ENST00000376237.8:c.*482+26_*482+27insG	ENSP00000365412.4:n.*482+26_*482+27insG
ENST00000383329.7:c.895+26_895+27insG	ENSP00000372819.3:n.895+26_895+27insG
ENST00000470363.5:n.213+26_213+27insG
ENST00000487245.5:n.1254+26_1254+27insG
NM_002117.5:c.895+26_895+27insG	NP_002108.4:n.895+26_895+27insG
NM_002117.6:c.895+26_895+27insG MANE Select	NP_002108.4:n.895+26_895+27insG