Canonical Allele Identifier: CA2677957665

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356743-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356744_31356745insTT , CM000668.2:g.31356744_31356745insTT	GRCh38
NC_000006.11:g.31324521_31324522insTT , CM000668.1:g.31324521_31324522insTT	GRCh37
NC_000006.10:g.31432500_31432501insTT	NCBI36
NG_023187.1:g.5469_5470insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1760_1761insAA
ENST00000481849.6:n.1760_1761insAA
ENST00000497377.6:n.1760_1761insAA
ENST00000640094.2:c.287_288insAA	ENSP00000491275.2:p.Thr97ArgfsTer?
ENST00000696558.1:c.287_288insAA	ENSP00000512716.1:p.Thr97ArgfsTer?
ENST00000696559.1:c.287_288insAA	ENSP00000512717.1:p.Thr97ArgfsTer?
ENST00000696560.1:c.287_288insAA	ENSP00000512718.1:p.Thr97ArgfsTer?
ENST00000696561.1:c.287_288insAA	ENSP00000512719.1:p.Thr97ArgfsTer?
ENST00000696562.1:c.287_288insAA	ENSP00000512720.1:p.Thr97ArgfsTer?
ENST00000412585.7:c.287_288insAA MANE Select	ENSP00000399168.2:p.Thr97ArgfsTer?
ENST00000412585.6:c.287_288insAA	ENSP00000399168.2:p.Thr97ArgfsTer?
ENST00000434333.1:c.320_321insAA	ENSP00000405931.1:p.Thr108ArgfsTer?
ENST00000474381.1:n.162_163insAA
ENST00000498007.1:n.308_309insAA
ENST00000603274.1:n.98_99insTT
NM_005514.6:c.287_288insAA	NP_005505.2:p.Thr97ArgfsTer?
XM_011514556.1:c.320_321insAA	XP_011512858.1:p.Thr108ArgfsTer?
XM_011514557.1:c.287_288insAA	XP_011512859.1:p.Thr97ArgfsTer?
XR_926175.1:n.297_298insAA
NM_005514.7:c.287_288insAA	NP_005505.2:p.Thr97ArgfsTer?
NM_005514.8:c.287_288insAA MANE Select	NP_005505.2:p.Thr97ArgfsTer?