Canonical Allele Identifier: CA2677957707
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356759_31356760insGTTGGTCTTGG , CM000668.2:g.31356759_31356760insGTTGGTCTTGG GRCh38
NC_000006.11:g.31324536_31324537insGTTGGTCTTGG , CM000668.1:g.31324536_31324537insGTTGGTCTTGG GRCh37
NC_000006.10:g.31432515_31432516insGTTGGTCTTGG NCBI36
NG_023187.1:g.5453_5454insCCAAGACCAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1744_1745insCCAAGACCAAC
ENST00000481849.6:n.1744_1745insCCAAGACCAAC
ENST00000497377.6:n.1744_1745insCCAAGACCAAC
ENST00000640094.2:c.271_272insCCAAGACCAAC ENSP00000491275.2:p.Tyr91SerfsTer?
ENST00000696558.1:c.271_272insCCAAGACCAAC ENSP00000512716.1:p.Tyr91SerfsTer?
ENST00000696559.1:c.271_272insCCAAGACCAAC ENSP00000512717.1:p.Tyr91SerfsTer?
ENST00000696560.1:c.271_272insCCAAGACCAAC ENSP00000512718.1:p.Tyr91SerfsTer?
ENST00000696561.1:c.271_272insCCAAGACCAAC ENSP00000512719.1:p.Tyr91SerfsTer?
ENST00000696562.1:c.271_272insCCAAGACCAAC ENSP00000512720.1:p.Tyr91SerfsTer?
ENST00000412585.7:c.271_272insCCAAGACCAAC MANE Select ENSP00000399168.2:p.Tyr91SerfsTer?
ENST00000412585.6:c.271_272insCCAAGACCAAC ENSP00000399168.2:p.Tyr91SerfsTer?
ENST00000434333.1:c.304_305insCCAAGACCAAC ENSP00000405931.1:p.Tyr102SerfsTer?
ENST00000474381.1:n.146_147insCCAAGACCAAC
ENST00000498007.1:n.292_293insCCAAGACCAAC
ENST00000603274.1:n.113_114insGTTGGTCTTGG
NM_005514.6:c.271_272insCCAAGACCAAC NP_005505.2:p.Tyr91SerfsTer?
XM_011514556.1:c.304_305insCCAAGACCAAC XP_011512858.1:p.Tyr102SerfsTer?
XM_011514557.1:c.271_272insCCAAGACCAAC XP_011512859.1:p.Tyr91SerfsTer?
XR_926175.1:n.281_282insCCAAGACCAAC
NM_005514.7:c.271_272insCCAAGACCAAC NP_005505.2:p.Tyr91SerfsTer?
NM_005514.8:c.271_272insCCAAGACCAAC MANE Select NP_005505.2:p.Tyr91SerfsTer?