Canonical Allele Identifier: CA2677950921

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270673-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270673_31270674insC , CM000668.2:g.31270673_31270674insC	GRCh38
NC_000006.11:g.31238450_31238451insC , CM000668.1:g.31238450_31238451insC	GRCh37
NC_000006.10:g.31346429_31346430insC	NCBI36
NG_029422.2:g.6458_6459insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-189_620-188insG MANE Select	ENSP00000365402.5:n.620-189_620-188insG
ENST00000376228.9:c.620-189_620-188insG	ENSP00000365402.5:n.620-189_620-188insG
ENST00000376237.8:c.*207-189_*207-188insG	ENSP00000365412.4:n.*207-189_*207-188insG
ENST00000383329.7:c.620-189_620-188insG	ENSP00000372819.3:n.620-189_620-188insG
ENST00000415537.1:c.618-189_618-188insG
ENST00000487245.5:n.979-189_979-188insG
ENST00000495835.1:n.809-189_809-188insG
NM_002117.5:c.620-189_620-188insG	NP_002108.4:n.620-189_620-188insG
NM_002117.6:c.620-189_620-188insG MANE Select	NP_002108.4:n.620-189_620-188insG