Canonical Allele Identifier: CA1619117488

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354626_31354630delinsCACTT , CM000668.2:g.31354626_31354630delinsCACTT	GRCh38
NC_000006.11:g.31322403_31322407delinsCACTT , CM000668.1:g.31322403_31322407delinsCACTT	GRCh37
NC_000006.10:g.31430382_31430386delinsCACTT	NCBI36
NG_023187.1:g.7583_7587delinsAAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3092+3_3092+7delinsAAGTG
ENST00000481849.6:n.3052+3_3052+7delinsAAGTG
ENST00000497377.6:n.2959+3_2959+7delinsAAGTG
ENST00000640094.2:c.928+3_928+7delinsAAGTG	ENSP00000491275.2:n.928+3_928+7delinsAAGTG
ENST00000696558.1:c.1114+3_1114+7delinsAAGTG	ENSP00000512716.1:n.1114+3_1114+7delinsAAGTG
ENST00000696559.1:c.1045+3_1045+7delinsAAGTG	ENSP00000512717.1:n.1045+3_1045+7delinsAAGTG
ENST00000696560.1:c.1045+3_1045+7delinsAAGTG	ENSP00000512718.1:n.1045+3_1045+7delinsAAGTG
ENST00000696561.1:c.1045+3_1045+7delinsAAGTG	ENSP00000512719.1:n.1045+3_1045+7delinsAAGTG
ENST00000696562.1:c.1045+3_1045+7delinsAAGTG	ENSP00000512720.1:n.1045+3_1045+7delinsAAGTG
ENST00000412585.7:c.1045+3_1045+7delinsAAGTG MANE Select	ENSP00000399168.2:n.1045+3_1045+7delinsAAGTG
ENST00000640094.1:c.121+3_121+7delinsAAGTG	ENSP00000491275.1:n.121+3_121+7delinsAAGTG
ENST00000412585.6:c.1045+3_1045+7delinsAAGTG	ENSP00000399168.2:n.1045+3_1045+7delinsAAGTG
ENST00000481849.5:n.177_181delinsAAGTG
ENST00000497377.5:n.444+3_444+7delinsAAGTG
NM_005514.6:c.1045+3_1045+7delinsAAGTG	NP_005505.2:n.1045+3_1045+7delinsAAGTG
XM_011514556.1:c.1078+3_1078+7delinsAAGTG	XP_011512858.1:n.1078+3_1078+7delinsAAGTG
XM_011514557.1:c.928+3_928+7delinsAAGTG	XP_011512859.1:n.928+3_928+7delinsAAGTG
XR_926175.1:n.1484+3_1484+7delinsAAGTG
NM_005514.7:c.1045+3_1045+7delinsAAGTG	NP_005505.2:n.1045+3_1045+7delinsAAGTG
NM_005514.8:c.1045+3_1045+7delinsAAGTG MANE Select	NP_005505.2:n.1045+3_1045+7delinsAAGTG