Canonical Allele Identifier: CA3710792
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs748394002

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271334_31271335insCCAAGT , CM000668.2:g.31271334_31271335insCCAAGT GRCh38
NC_000006.11:g.31239111_31239112insCCAAGT , CM000668.1:g.31239111_31239112insCCAAGT GRCh37
NC_000006.10:g.31347090_31347091insCCAAGT NCBI36
NG_029422.2:g.5797_5798insACTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.357_358insACTTGG MANE Select ENSP00000365402.5:p.Leu119_Gln120insThrTr...
ENST00000376228.9:c.357_358insACTTGG ENSP00000365402.5:p.Leu119_Gln120insThrTr...
ENST00000376237.8:c.344-4_344-3insACTTGG ENSP00000365412.4:n.344-4_344-3insACTTGG
ENST00000383329.7:c.357_358insACTTGG ENSP00000372819.3:p.Leu119_Gln120insThrTr...
ENST00000415537.1:c.355_356insACTTGG
ENST00000484378.1:n.626_627insACTTGG
ENST00000487245.5:n.716_717insACTTGG
ENST00000495835.1:n.546_547insACTTGG
NM_002117.5:c.357_358insACTTGG NP_002108.4:p.Leu119_Gln120insThrTrp
NM_002117.6:c.357_358insACTTGG MANE Select NP_002108.4:p.Leu119_Gln120insThrTrp