Canonical Allele Identifier: CA2677956938
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356432_31356433insAT , CM000668.2:g.31356432_31356433insAT GRCh38
NC_000006.11:g.31324209_31324210insAT , CM000668.1:g.31324209_31324210insAT GRCh37
NC_000006.10:g.31432188_31432189insAT NCBI36
NG_023187.1:g.5780_5781insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1826_1827insAT
ENST00000481849.6:n.1826_1827insAT
ENST00000497377.6:n.1826_1827insAT
ENST00000640094.2:c.353_354insAT ENSP00000491275.2:p.Leu119SerfsTer?
ENST00000696558.1:c.353_354insAT ENSP00000512716.1:p.Leu119SerfsTer?
ENST00000696559.1:c.353_354insAT ENSP00000512717.1:p.Leu119SerfsTer?
ENST00000696560.1:c.353_354insAT ENSP00000512718.1:p.Leu119SerfsTer?
ENST00000696561.1:c.353_354insAT ENSP00000512719.1:p.Leu119SerfsTer?
ENST00000696562.1:c.353_354insAT ENSP00000512720.1:p.Leu119SerfsTer?
ENST00000412585.7:c.353_354insAT MANE Select ENSP00000399168.2:p.Leu119SerfsTer?
ENST00000412585.6:c.353_354insAT ENSP00000399168.2:p.Leu119SerfsTer?
ENST00000434333.1:c.386_387insAT ENSP00000405931.1:p.Leu130SerfsTer?
ENST00000474381.1:n.228_229insAT
ENST00000498007.1:n.619_620insAT
NM_005514.6:c.353_354insAT NP_005505.2:p.Leu119SerfsTer?
XM_011514556.1:c.386_387insAT XP_011512858.1:p.Leu130SerfsTer?
XM_011514557.1:c.353_354insAT XP_011512859.1:p.Leu119SerfsTer?
XR_926175.1:n.363_364insAT
NM_005514.7:c.353_354insAT NP_005505.2:p.Leu119SerfsTer?
NM_005514.8:c.353_354insAT MANE Select NP_005505.2:p.Leu119SerfsTer?