Canonical Allele Identifier: CA1618450433

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792565_29792586delinsAGGATGGAGCCGCGGGCGCCGT , CM000668.2:g.29792565_29792586delinsAGGATGGAGCCGCGGGCGCCGT GRCh38
NC_000006.11:g.29760342_29760363delinsAGGATGGAGCCGCGGGCGCCGT , CM000668.1:g.29760342_29760363delinsAGGATGGAGCCGCGGGCGCCGT GRCh37
NC_000006.10:g.29868321_29868342delinsAGGATGGAGCCGCGGGCGCCGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.165_186delinsACGGCGCCCGCGGCTCCATCCT (HCG4)
ENST00000429037.2:n.201_222delinsAGGATGGAGCCGCGGGCGCCGT (HLA-V)
ENST00000446817.1:n.311_332delinsAGGATGGAGCCGCGGGCGCCGT (HLA-V)
ENST00000457107.5:n.212_233delinsAGGATGGAGCCGCGGGCGCCGT (HLA-V)
ENST00000476601.5:n.529_550delinsAGGATGGAGCCGCGGGCGCCGT (HLA-V)
NM_001207043.1:c.427_448delinsAGGATGGAGCCGCGGGCGCCGT NP_001193972.1:p.Arg143=
NR_002139.2:n.488_509delinsACGGCGCCCGCGGCTCCATCCT (HCG4)
NR_132323.1:n.529_550delinsAGGATGGAGCCGCGGGCGCCGT