Canonical Allele Identifier: CA1619078440
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761150750
gnomAD v4: 6-31269820-TAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269821_31269822del , CM000668.2:g.31269821_31269822del GRCh38
NC_000006.11:g.31237598_31237599del , CM000668.1:g.31237598_31237599del GRCh37
NC_000006.10:g.31345577_31345578del NCBI36
NG_029422.2:g.7310_7311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+144_1015+145del MANE Select ENSP00000365402.5:n.1015+144_1015+145del
ENST00000376228.9:c.1015+144_1015+145del ENSP00000365402.5:n.1015+144_1015+145del
ENST00000376237.8:c.*602+144_*602+145del ENSP00000365412.4:n.*602+144_*602+145del
ENST00000383329.7:c.1015+144_1015+145del ENSP00000372819.3:n.1015+144_1015+145del
ENST00000470363.5:n.477_478del
ENST00000487245.5:n.1374+144_1374+145del
NM_002117.5:c.1015+144_1015+145del NP_002108.4:n.1015+144_1015+145del
NM_002117.6:c.1015+144_1015+145del MANE Select NP_002108.4:n.1015+144_1015+145del
Search 100 bp 5'
Search 100 bp 3'