Canonical Allele Identifier: CA1619112323

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356489_31356494delinsCCCCGA , CM000668.2:g.31356489_31356494delinsCCCCGA	GRCh38
NC_000006.11:g.31324266_31324271delinsCCCCGA , CM000668.1:g.31324266_31324271delinsCCCCGA	GRCh37
NC_000006.10:g.31432245_31432250delinsCCCCGA	NCBI36
NG_023187.1:g.5719_5724delinsTCGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1817-52_1817-47delinsTCGGGG
ENST00000481849.6:n.1817-52_1817-47delinsTCGGGG
ENST00000497377.6:n.1817-52_1817-47delinsTCGGGG
ENST00000640094.2:c.344-52_344-47delinsTCGGGG	ENSP00000491275.2:n.344-52_344-47delinsTCGGGG
ENST00000696558.1:c.344-52_344-47delinsTCGGGG	ENSP00000512716.1:n.344-52_344-47delinsTCGGGG
ENST00000696559.1:c.344-52_344-47delinsTCGGGG	ENSP00000512717.1:n.344-52_344-47delinsTCGGGG
ENST00000696560.1:c.344-52_344-47delinsTCGGGG	ENSP00000512718.1:n.344-52_344-47delinsTCGGGG
ENST00000696561.1:c.344-52_344-47delinsTCGGGG	ENSP00000512719.1:n.344-52_344-47delinsTCGGGG
ENST00000696562.1:c.344-52_344-47delinsTCGGGG	ENSP00000512720.1:n.344-52_344-47delinsTCGGGG
ENST00000412585.7:c.344-52_344-47delinsTCGGGG MANE Select	ENSP00000399168.2:n.344-52_344-47delinsTCGGGG
ENST00000412585.6:c.344-52_344-47delinsTCGGGG	ENSP00000399168.2:n.344-52_344-47delinsTCGGGG
ENST00000434333.1:c.377-52_377-47delinsTCGGGG	ENSP00000405931.1:n.377-52_377-47delinsTCGGGG
ENST00000474381.1:n.219-52_219-47delinsTCGGGG
ENST00000498007.1:n.558_563delinsTCGGGG
NM_005514.6:c.344-52_344-47delinsTCGGGG	NP_005505.2:n.344-52_344-47delinsTCGGGG
XM_011514556.1:c.377-52_377-47delinsTCGGGG	XP_011512858.1:n.377-52_377-47delinsTCGGGG
XM_011514557.1:c.344-52_344-47delinsTCGGGG	XP_011512859.1:n.344-52_344-47delinsTCGGGG
XR_926175.1:n.354-52_354-47delinsTCGGGG
NM_005514.7:c.344-52_344-47delinsTCGGGG	NP_005505.2:n.344-52_344-47delinsTCGGGG
NM_005514.8:c.344-52_344-47delinsTCGGGG MANE Select	NP_005505.2:n.344-52_344-47delinsTCGGGG