Canonical Allele Identifier: CA1619112988

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356748_31356751delinsCCTG , CM000668.2:g.31356748_31356751delinsCCTG	GRCh38
NC_000006.11:g.31324525_31324528delinsCCTG , CM000668.1:g.31324525_31324528delinsCCTG	GRCh37
NC_000006.10:g.31432504_31432507delinsCCTG	NCBI36
NG_023187.1:g.5462_5465delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1753_1756delinsCAGG
ENST00000481849.6:n.1753_1756delinsCAGG
ENST00000497377.6:n.1753_1756delinsCAGG
ENST00000640094.2:c.280_283delinsCAGG	ENSP00000491275.2:p.Gln94=
ENST00000696558.1:c.280_283delinsCAGG	ENSP00000512716.1:p.Gln94=
ENST00000696559.1:c.280_283delinsCAGG	ENSP00000512717.1:p.Gln94=
ENST00000696560.1:c.280_283delinsCAGG	ENSP00000512718.1:p.Gln94=
ENST00000696561.1:c.280_283delinsCAGG	ENSP00000512719.1:p.Gln94=
ENST00000696562.1:c.280_283delinsCAGG	ENSP00000512720.1:p.Gln94=
ENST00000412585.7:c.280_283delinsCAGG MANE Select	ENSP00000399168.2:p.Gln94=
ENST00000412585.6:c.280_283delinsCAGG	ENSP00000399168.2:p.Gln94=
ENST00000434333.1:c.313_316delinsCAGG	ENSP00000405931.1:p.Gln105=
ENST00000474381.1:n.155_158delinsCAGG
ENST00000498007.1:n.301_304delinsCAGG
ENST00000603274.1:n.102_105delinsCCTG
NM_005514.6:c.280_283delinsCAGG	NP_005505.2:p.Gln94=
XM_011514556.1:c.313_316delinsCAGG	XP_011512858.1:p.Gln105=
XM_011514557.1:c.280_283delinsCAGG	XP_011512859.1:p.Gln94=
XR_926175.1:n.290_293delinsCAGG
NM_005514.7:c.280_283delinsCAGG	NP_005505.2:p.Gln94=
NM_005514.8:c.280_283delinsCAGG MANE Select	NP_005505.2:p.Gln94=