Canonical Allele Identifier: CA136862558

Gene: HLA-C

Linked Data

• dbSNP Id: rs796156244

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269990_31269997delinsCAACAGCC , CM000668.2:g.31269990_31269997delinsCAACAGCC	GRCh38
NC_000006.11:g.31237767_31237774delinsCAACAGCC , CM000668.1:g.31237767_31237774delinsCAACAGCC	GRCh37
NC_000006.10:g.31345746_31345753delinsCAACAGCC	NCBI36
NG_029422.2:g.7135_7142delinsGGCTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.984_991delinsGGCTGTTG MANE Select	ENSP00000365402.5:p.Thr329_Met331delinsAlaValVal
ENST00000376228.9:c.984_991delinsGGCTGTTG	ENSP00000365402.5:p.Thr329_Met331delinsAlaValVal
ENST00000376237.8:c.*571_*578delinsGGCTGTTG	ENSP00000365412.4:n.*571_*578delinsGGCTGTTG
ENST00000383329.7:c.984_991delinsGGCTGTTG	ENSP00000372819.3:p.Thr329_Met331delinsAlaValVal
ENST00000470363.5:n.302_309delinsGGCTGTTG
ENST00000487245.5:n.1343_1350delinsGGCTGTTG
NM_002117.5:c.984_991delinsGGCTGTTG	NP_002108.4:p.Thr329_Met331delinsAlaValVal
NM_002117.6:c.984_991delinsGGCTGTTG MANE Select	NP_002108.4:p.Thr329_Met331delinsAlaValVal