Canonical Allele Identifier: CA2677951725
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271674_31271675insGGAGAT , CM000668.2:g.31271674_31271675insGGAGAT GRCh38
NC_000006.11:g.31239451_31239452insGGAGAT , CM000668.1:g.31239451_31239452insGGAGAT GRCh37
NC_000006.10:g.31347430_31347431insGGAGAT NCBI36
NG_029422.2:g.5458_5459insTCTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.268_269insTCTCCA MANE Select ENSP00000365402.5:p.Gln89_Lys90insIleSer
ENST00000376228.9:c.268_269insTCTCCA ENSP00000365402.5:p.Gln89_Lys90insIleSer
ENST00000376237.8:c.268_269insTCTCCA ENSP00000365412.4:p.Gln89_Lys90insIleSer
ENST00000383329.7:c.268_269insTCTCCA ENSP00000372819.3:p.Gln89_Lys90insIleSer
ENST00000415537.1:c.266_267insTCTCCA
ENST00000484378.1:n.287_288insTCTCCA
ENST00000487245.5:n.377_378insTCTCCA
ENST00000495835.1:n.457_458insTCTCCA
NM_002117.5:c.268_269insTCTCCA NP_002108.4:p.Gln89_Lys90insIleSer
NM_002117.6:c.268_269insTCTCCA MANE Select NP_002108.4:p.Gln89_Lys90insIleSer