Canonical Allele Identifier: CA2677951017

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270779-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270784_31270785del , CM000668.2:g.31270784_31270785del	GRCh38
NC_000006.11:g.31238561_31238562del , CM000668.1:g.31238561_31238562del	GRCh37
NC_000006.10:g.31346540_31346541del	NCBI36
NG_029422.2:g.6351_6352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.619+292_619+293del MANE Select	ENSP00000365402.5:n.619+292_619+293del
ENST00000376228.9:c.619+292_619+293del	ENSP00000365402.5:n.619+292_619+293del
ENST00000376237.8:c.*206+292_*206+293del	ENSP00000365412.4:n.*206+292_*206+293del
ENST00000383329.7:c.619+292_619+293del	ENSP00000372819.3:n.619+292_619+293del
ENST00000415537.1:c.617+292_617+293del
ENST00000487245.5:n.978+292_978+293del
ENST00000495835.1:n.808+292_808+293del
NM_002117.5:c.619+292_619+293del	NP_002108.4:n.619+292_619+293del
NM_002117.6:c.619+292_619+293del MANE Select	NP_002108.4:n.619+292_619+293del