Canonical Allele Identifier: CA1619080703
Gene: HLA-C HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271561_31271564delinsAGGG , CM000668.2:g.31271561_31271564delinsAGGG GRCh38
NC_000006.11:g.31239338_31239341delinsAGGG , CM000668.1:g.31239338_31239341delinsAGGG GRCh37
NC_000006.10:g.31347317_31347320delinsAGGG NCBI36
NG_029422.2:g.5568_5571delinsCCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+35_343+38delinsCCCT MANE Select ENSP00000365402.5:n.343+35_343+38delinsCC...
ENST00000376228.9:c.343+35_343+38delinsCCCT ENSP00000365402.5:n.343+35_343+38delinsCC...
ENST00000376237.8:c.343+35_343+38delinsCCCT ENSP00000365412.4:n.343+35_343+38delinsCC...
ENST00000383329.7:c.343+35_343+38delinsCCCT ENSP00000372819.3:n.343+35_343+38delinsCC...
ENST00000415537.1:c.341+35_341+38delinsCCCT
ENST00000484378.1:n.397_400delinsCCCT
ENST00000487245.5:n.487_490delinsCCCT
ENST00000495835.1:n.532+35_532+38delinsCCCT
NM_002117.5:c.343+35_343+38delinsCCCT NP_002108.4:n.343+35_343+38delinsCCCT
NM_002117.6:c.343+35_343+38delinsCCCT MANE Select NP_002108.4:n.343+35_343+38delinsCCCT
Search 100 bp 5'
Search 100 bp 3'