Canonical Allele Identifier: CA2677951408
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271377-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271377_31271378insT , CM000668.2:g.31271377_31271378insT GRCh38
NC_000006.11:g.31239154_31239155insT , CM000668.1:g.31239154_31239155insT GRCh37
NC_000006.10:g.31347133_31347134insT NCBI36
NG_029422.2:g.5754_5755insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-30_344-29insA MANE Select ENSP00000365402.5:n.344-30_344-29insA
ENST00000376228.9:c.344-30_344-29insA ENSP00000365402.5:n.344-30_344-29insA
ENST00000376237.8:c.344-47_344-46insA ENSP00000365412.4:n.344-47_344-46insA
ENST00000383329.7:c.344-30_344-29insA ENSP00000372819.3:n.344-30_344-29insA
ENST00000415537.1:c.342-30_342-29insA
ENST00000484378.1:n.583_584insA
ENST00000487245.5:n.673_674insA
ENST00000495835.1:n.533-30_533-29insA
NM_002117.5:c.344-30_344-29insA NP_002108.4:n.344-30_344-29insA
NM_002117.6:c.344-30_344-29insA MANE Select NP_002108.4:n.344-30_344-29insA
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Search 100 bp 3'