Canonical Allele Identifier: CA2677957700
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356757_31356758insAAT , CM000668.2:g.31356757_31356758insAAT GRCh38
NC_000006.11:g.31324534_31324535insAAT , CM000668.1:g.31324534_31324535insAAT GRCh37
NC_000006.10:g.31432513_31432514insAAT NCBI36
NG_023187.1:g.5456_5457insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1747_1748insTTA
ENST00000481849.6:n.1747_1748insTTA
ENST00000497377.6:n.1747_1748insTTA
ENST00000640094.2:c.274_275insTTA ENSP00000491275.2:p.Tyr91_Lys92insIle
ENST00000696558.1:c.274_275insTTA ENSP00000512716.1:p.Tyr91_Lys92insIle
ENST00000696559.1:c.274_275insTTA ENSP00000512717.1:p.Tyr91_Lys92insIle
ENST00000696560.1:c.274_275insTTA ENSP00000512718.1:p.Tyr91_Lys92insIle
ENST00000696561.1:c.274_275insTTA ENSP00000512719.1:p.Tyr91_Lys92insIle
ENST00000696562.1:c.274_275insTTA ENSP00000512720.1:p.Tyr91_Lys92insIle
ENST00000412585.7:c.274_275insTTA MANE Select ENSP00000399168.2:p.Tyr91_Lys92insIle
ENST00000412585.6:c.274_275insTTA ENSP00000399168.2:p.Tyr91_Lys92insIle
ENST00000434333.1:c.307_308insTTA ENSP00000405931.1:p.Tyr102_Lys103insIle
ENST00000474381.1:n.149_150insTTA
ENST00000498007.1:n.295_296insTTA
ENST00000603274.1:n.111_112insAAT
NM_005514.6:c.274_275insTTA NP_005505.2:p.Tyr91_Lys92insIle
XM_011514556.1:c.307_308insTTA XP_011512858.1:p.Tyr102_Lys103insIle
XM_011514557.1:c.274_275insTTA XP_011512859.1:p.Tyr91_Lys92insIle
XR_926175.1:n.284_285insTTA
NM_005514.7:c.274_275insTTA NP_005505.2:p.Tyr91_Lys92insIle
NM_005514.8:c.274_275insTTA MANE Select NP_005505.2:p.Tyr91_Lys92insIle