Canonical Allele Identifier: CA2677957653

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356729-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356730_31356732del , CM000668.2:g.31356730_31356732del	GRCh38
NC_000006.11:g.31324507_31324509del , CM000668.1:g.31324507_31324509del	GRCh37
NC_000006.10:g.31432486_31432488del	NCBI36
NG_023187.1:g.5481_5483del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1772_1774del
ENST00000481849.6:n.1772_1774del
ENST00000497377.6:n.1772_1774del
ENST00000640094.2:c.299_301del	ENSP00000491275.2:p.Glu100_Ser101delinsGly
ENST00000696558.1:c.299_301del	ENSP00000512716.1:p.Glu100_Ser101delinsGly
ENST00000696559.1:c.299_301del	ENSP00000512717.1:p.Glu100_Ser101delinsGly
ENST00000696560.1:c.299_301del	ENSP00000512718.1:p.Glu100_Ser101delinsGly
ENST00000696561.1:c.299_301del	ENSP00000512719.1:p.Glu100_Ser101delinsGly
ENST00000696562.1:c.299_301del	ENSP00000512720.1:p.Glu100_Ser101delinsGly
ENST00000412585.7:c.299_301del MANE Select	ENSP00000399168.2:p.Glu100_Ser101delinsGly
ENST00000412585.6:c.299_301del	ENSP00000399168.2:p.Glu100_Ser101delinsGly
ENST00000434333.1:c.332_334del	ENSP00000405931.1:p.Glu111_Ser112delinsGly
ENST00000474381.1:n.174_176del
ENST00000498007.1:n.320_322del
ENST00000603274.1:n.84_86del
NM_005514.6:c.299_301del	NP_005505.2:p.Glu100_Ser101delinsGly
XM_011514556.1:c.332_334del	XP_011512858.1:p.Glu111_Ser112delinsGly
XM_011514557.1:c.299_301del	XP_011512859.1:p.Glu100_Ser101delinsGly
XR_926175.1:n.309_311del
NM_005514.7:c.299_301del	NP_005505.2:p.Glu100_Ser101delinsGly
NM_005514.8:c.299_301del MANE Select	NP_005505.2:p.Glu100_Ser101delinsGly