Canonical Allele Identifier: CA1087469691
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356780_31356781insGTATCATTAA , CM000668.2:g.31356780_31356781insGTATCATTAA GRCh38
NC_000006.11:g.31324557_31324558insGTATCATTAA , CM000668.1:g.31324557_31324558insGTATCATTAA GRCh37
NC_000006.10:g.31432536_31432537insGTATCATTAA NCBI36
NG_023187.1:g.5432_5433insTTAATGATAC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1723_1724insTTAATGATAC
ENST00000481849.6:n.1723_1724insTTAATGATAC
ENST00000497377.6:n.1723_1724insTTAATGATAC
ENST00000640094.2:c.250_251insTTAATGATAC ENSP00000491275.2:p.Trp84PhefsTer18
ENST00000696558.1:c.250_251insTTAATGATAC ENSP00000512716.1:p.Trp84PhefsTer18
ENST00000696559.1:c.250_251insTTAATGATAC ENSP00000512717.1:p.Trp84PhefsTer18
ENST00000696560.1:c.250_251insTTAATGATAC ENSP00000512718.1:p.Trp84PhefsTer18
ENST00000696561.1:c.250_251insTTAATGATAC ENSP00000512719.1:p.Trp84PhefsTer18
ENST00000696562.1:c.250_251insTTAATGATAC ENSP00000512720.1:p.Trp84PhefsTer18
ENST00000412585.7:c.250_251insTTAATGATAC MANE Select ENSP00000399168.2:p.Trp84PhefsTer18
ENST00000412585.6:c.250_251insTTAATGATAC ENSP00000399168.2:p.Trp84PhefsTer18
ENST00000434333.1:c.283_284insTTAATGATAC ENSP00000405931.1:p.Trp95PhefsTer18
ENST00000474381.1:n.125_126insTTAATGATAC
ENST00000498007.1:n.271_272insTTAATGATAC
ENST00000603274.1:n.134_135insGTATCATTAA
NM_005514.6:c.250_251insTTAATGATAC NP_005505.2:p.Trp84PhefsTer18
XM_011514556.1:c.283_284insTTAATGATAC XP_011512858.1:p.Trp95PhefsTer18
XM_011514557.1:c.250_251insTTAATGATAC XP_011512859.1:p.Trp84PhefsTer18
XR_926175.1:n.260_261insTTAATGATAC
NM_005514.7:c.250_251insTTAATGATAC NP_005505.2:p.Trp84PhefsTer18
NM_005514.8:c.250_251insTTAATGATAC MANE Select NP_005505.2:p.Trp84PhefsTer18