Canonical Allele Identifier: CA2770503815

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356425_31356427del , CM000668.2:g.31356425_31356427del	GRCh38
NC_000006.11:g.31324202_31324204del , CM000668.1:g.31324202_31324204del	GRCh37
NC_000006.10:g.31432181_31432183del	NCBI36
NG_023187.1:g.5786_5788del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1832_1834del
ENST00000481849.6:n.1832_1834del
ENST00000497377.6:n.1832_1834del
ENST00000640094.2:c.359_361del	ENSP00000491275.2:p.Gln120_Ser121delinsArg
ENST00000696558.1:c.359_361del	ENSP00000512716.1:p.Gln120_Ser121delinsArg
ENST00000696559.1:c.359_361del	ENSP00000512717.1:p.Gln120_Ser121delinsArg
ENST00000696560.1:c.359_361del	ENSP00000512718.1:p.Gln120_Ser121delinsArg
ENST00000696561.1:c.359_361del	ENSP00000512719.1:p.Gln120_Ser121delinsArg
ENST00000696562.1:c.359_361del	ENSP00000512720.1:p.Gln120_Ser121delinsArg
ENST00000412585.7:c.359_361del MANE Select	ENSP00000399168.2:p.Gln120_Ser121delinsArg
ENST00000412585.6:c.359_361del	ENSP00000399168.2:p.Gln120_Ser121delinsArg
ENST00000434333.1:c.392_394del	ENSP00000405931.1:p.Gln131_Ser132delinsArg
ENST00000474381.1:n.234_236del
ENST00000498007.1:n.625_627del
NM_005514.6:c.359_361del	NP_005505.2:p.Gln120_Ser121delinsArg
XM_011514556.1:c.392_394del	XP_011512858.1:p.Gln131_Ser132delinsArg
XM_011514557.1:c.359_361del	XP_011512859.1:p.Gln120_Ser121delinsArg
XR_926175.1:n.369_371del
NM_005514.7:c.359_361del	NP_005505.2:p.Gln120_Ser121delinsArg
NM_005514.8:c.359_361del MANE Select	NP_005505.2:p.Gln120_Ser121delinsArg