Canonical Allele Identifier: CA2677950900

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270660-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270662_31270663del , CM000668.2:g.31270662_31270663del	GRCh38
NC_000006.11:g.31238439_31238440del , CM000668.1:g.31238439_31238440del	GRCh37
NC_000006.10:g.31346418_31346419del	NCBI36
NG_029422.2:g.6470_6471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-177_620-176del MANE Select	ENSP00000365402.5:n.620-177_620-176del
ENST00000376228.9:c.620-177_620-176del	ENSP00000365402.5:n.620-177_620-176del
ENST00000376237.8:c.*207-177_*207-176del	ENSP00000365412.4:n.*207-177_*207-176del
ENST00000383329.7:c.620-177_620-176del	ENSP00000372819.3:n.620-177_620-176del
ENST00000415537.1:c.618-177_618-176del
ENST00000487245.5:n.979-177_979-176del
ENST00000495835.1:n.809-177_809-176del
NM_002117.5:c.620-177_620-176del	NP_002108.4:n.620-177_620-176del
NM_002117.6:c.620-177_620-176del MANE Select	NP_002108.4:n.620-177_620-176del