Canonical Allele Identifier: CA2677950958

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113907849
• gnomAD v4: 6-31270715-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270715_31270716insGA , CM000668.2:g.31270715_31270716insGA	GRCh38
NC_000006.11:g.31238492_31238493insGA , CM000668.1:g.31238492_31238493insGA	GRCh37
NC_000006.10:g.31346471_31346472insGA	NCBI36
NG_029422.2:g.6416_6417insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-231_620-230insTC MANE Select	ENSP00000365402.5:n.620-231_620-230insTC
ENST00000376228.9:c.620-231_620-230insTC	ENSP00000365402.5:n.620-231_620-230insTC
ENST00000376237.8:c.*207-231_*207-230insTC	ENSP00000365412.4:n.*207-231_*207-230insTC
ENST00000383329.7:c.620-231_620-230insTC	ENSP00000372819.3:n.620-231_620-230insTC
ENST00000415537.1:c.618-231_618-230insTC
ENST00000487245.5:n.979-231_979-230insTC
ENST00000495835.1:n.809-231_809-230insTC
NM_002117.5:c.620-231_620-230insTC	NP_002108.4:n.620-231_620-230insTC
NM_002117.6:c.620-231_620-230insTC MANE Select	NP_002108.4:n.620-231_620-230insTC