Canonical Allele Identifier: CA2677957713
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356759_31356760insTGGTCTTGA , CM000668.2:g.31356759_31356760insTGGTCTTGA GRCh38
NC_000006.11:g.31324536_31324537insTGGTCTTGA , CM000668.1:g.31324536_31324537insTGGTCTTGA GRCh37
NC_000006.10:g.31432515_31432516insTGGTCTTGA NCBI36
NG_023187.1:g.5453_5454insTCAAGACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1744_1745insTCAAGACCA
ENST00000481849.6:n.1744_1745insTCAAGACCA
ENST00000497377.6:n.1744_1745insTCAAGACCA
ENST00000640094.2:c.271_272insTCAAGACCA ENSP00000491275.2:p.Tyr91delinsPheLysThrAsn
ENST00000696558.1:c.271_272insTCAAGACCA ENSP00000512716.1:p.Tyr91delinsPheLysThrAsn
ENST00000696559.1:c.271_272insTCAAGACCA ENSP00000512717.1:p.Tyr91delinsPheLysThrAsn
ENST00000696560.1:c.271_272insTCAAGACCA ENSP00000512718.1:p.Tyr91delinsPheLysThrAsn
ENST00000696561.1:c.271_272insTCAAGACCA ENSP00000512719.1:p.Tyr91delinsPheLysThrAsn
ENST00000696562.1:c.271_272insTCAAGACCA ENSP00000512720.1:p.Tyr91delinsPheLysThrAsn
ENST00000412585.7:c.271_272insTCAAGACCA MANE Select ENSP00000399168.2:p.Tyr91delinsPheLysThrAsn
ENST00000412585.6:c.271_272insTCAAGACCA ENSP00000399168.2:p.Tyr91delinsPheLysThrAsn
ENST00000434333.1:c.304_305insTCAAGACCA ENSP00000405931.1:p.Tyr102delinsPheLysThrAsn
ENST00000474381.1:n.146_147insTCAAGACCA
ENST00000498007.1:n.292_293insTCAAGACCA
ENST00000603274.1:n.113_114insTGGTCTTGA
NM_005514.6:c.271_272insTCAAGACCA NP_005505.2:p.Tyr91delinsPheLysThrAsn
XM_011514556.1:c.304_305insTCAAGACCA XP_011512858.1:p.Tyr102delinsPheLysThrAsn
XM_011514557.1:c.271_272insTCAAGACCA XP_011512859.1:p.Tyr91delinsPheLysThrAsn
XR_926175.1:n.281_282insTCAAGACCA
NM_005514.7:c.271_272insTCAAGACCA NP_005505.2:p.Tyr91delinsPheLysThrAsn
NM_005514.8:c.271_272insTCAAGACCA MANE Select NP_005505.2:p.Tyr91delinsPheLysThrAsn