Canonical Allele Identifier: CA2770503826

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356493_31356494insCCCAG , CM000668.2:g.31356493_31356494insCCCAG	GRCh38
NC_000006.11:g.31324270_31324271insCCCAG , CM000668.1:g.31324270_31324271insCCCAG	GRCh37
NC_000006.10:g.31432249_31432250insCCCAG	NCBI36
NG_023187.1:g.5720_5721insTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-51_1817-50insTGGGC
ENST00000481849.6:n.1817-51_1817-50insTGGGC
ENST00000497377.6:n.1817-51_1817-50insTGGGC
ENST00000640094.2:c.344-51_344-50insTGGGC	ENSP00000491275.2:n.344-51_344-50insTGGGC
ENST00000696558.1:c.344-51_344-50insTGGGC	ENSP00000512716.1:n.344-51_344-50insTGGGC
ENST00000696559.1:c.344-51_344-50insTGGGC	ENSP00000512717.1:n.344-51_344-50insTGGGC
ENST00000696560.1:c.344-51_344-50insTGGGC	ENSP00000512718.1:n.344-51_344-50insTGGGC
ENST00000696561.1:c.344-51_344-50insTGGGC	ENSP00000512719.1:n.344-51_344-50insTGGGC
ENST00000696562.1:c.344-51_344-50insTGGGC	ENSP00000512720.1:n.344-51_344-50insTGGGC
ENST00000412585.7:c.344-51_344-50insTGGGC MANE Select	ENSP00000399168.2:n.344-51_344-50insTGGGC
ENST00000412585.6:c.344-51_344-50insTGGGC	ENSP00000399168.2:n.344-51_344-50insTGGGC
ENST00000434333.1:c.377-51_377-50insTGGGC	ENSP00000405931.1:n.377-51_377-50insTGGGC
ENST00000474381.1:n.219-51_219-50insTGGGC
ENST00000498007.1:n.559_560insTGGGC
NM_005514.6:c.344-51_344-50insTGGGC	NP_005505.2:n.344-51_344-50insTGGGC
XM_011514556.1:c.377-51_377-50insTGGGC	XP_011512858.1:n.377-51_377-50insTGGGC
XM_011514557.1:c.344-51_344-50insTGGGC	XP_011512859.1:n.344-51_344-50insTGGGC
XR_926175.1:n.354-51_354-50insTGGGC
NM_005514.7:c.344-51_344-50insTGGGC	NP_005505.2:n.344-51_344-50insTGGGC
NM_005514.8:c.344-51_344-50insTGGGC MANE Select	NP_005505.2:n.344-51_344-50insTGGGC