Canonical Allele Identifier: CA2677956564
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356181_31356182insCTCCTTCCCG , CM000668.2:g.31356181_31356182insCTCCTTCCCG GRCh38
NC_000006.11:g.31323958_31323959insCTCCTTCCCG , CM000668.1:g.31323958_31323959insCTCCTTCCCG GRCh37
NC_000006.10:g.31431937_31431938insCTCCTTCCCG NCBI36
NG_023187.1:g.6031_6032insCGGGAAGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2077_2078insCGGGAAGGAG
ENST00000481849.6:n.2077_2078insCGGGAAGGAG
ENST00000497377.6:n.2077_2078insCGGGAAGGAG
ENST00000640094.2:c.604_605insCGGGAAGGAG ENSP00000491275.2:p.Lys202ThrfsTer9
ENST00000696558.1:c.604_605insCGGGAAGGAG ENSP00000512716.1:p.Lys202ThrfsTer9
ENST00000696559.1:c.604_605insCGGGAAGGAG ENSP00000512717.1:p.Lys202ThrfsTer9
ENST00000696560.1:c.604_605insCGGGAAGGAG ENSP00000512718.1:p.Lys202ThrfsTer9
ENST00000696561.1:c.604_605insCGGGAAGGAG ENSP00000512719.1:p.Lys202ThrfsTer9
ENST00000696562.1:c.604_605insCGGGAAGGAG ENSP00000512720.1:p.Lys202ThrfsTer9
ENST00000412585.7:c.604_605insCGGGAAGGAG MANE Select ENSP00000399168.2:p.Lys202ThrfsTer9
ENST00000412585.6:c.604_605insCGGGAAGGAG ENSP00000399168.2:p.Lys202ThrfsTer9
ENST00000434333.1:c.637_638insCGGGAAGGAG ENSP00000405931.1:p.Lys213ThrfsTer9
ENST00000474381.1:n.479_480insCGGGAAGGAG
ENST00000498007.1:n.870_871insCGGGAAGGAG
NM_005514.6:c.604_605insCGGGAAGGAG NP_005505.2:p.Lys202ThrfsTer9
XM_011514556.1:c.637_638insCGGGAAGGAG XP_011512858.1:p.Lys213ThrfsTer9
XM_011514557.1:c.604_605insCGGGAAGGAG XP_011512859.1:p.Lys202ThrfsTer9
XR_926175.1:n.614_615insCGGGAAGGAG
NM_005514.7:c.604_605insCGGGAAGGAG NP_005505.2:p.Lys202ThrfsTer9
NM_005514.8:c.604_605insCGGGAAGGAG MANE Select NP_005505.2:p.Lys202ThrfsTer9