Canonical Allele Identifier: CA2834601268

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354415_31354416insGCCCCCAGGCCCCCCCC , CM000668.2:g.31354415_31354416insGCCCCCAGGCCCCCCCC	GRCh38
NC_000006.11:g.31322192_31322193insGCCCCCAGGCCCCCCCC , CM000668.1:g.31322192_31322193insGCCCCCAGGCCCCCCCC	GRCh37
NC_000006.10:g.31430171_31430172insGCCCCCAGGCCCCCCCC	NCBI36
NG_023187.1:g.7797_7798insGGGGGGGGCCTGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+63_3140+64insGGGGGGGGCCTGGGGGC
ENST00000481849.6:n.3100+63_3100+64insGGGGGGGGCCTGGGGGC
ENST00000497377.6:n.3007+63_3007+64insGGGGGGGGCCTGGGGGC
ENST00000696558.1:c.1162+63_1162+64insGGGGGGGGCCTGGGGGC	ENSP00000512716.1:n.1162+63_1162+64insGGGGGGGGCCTGGGGGC
ENST00000696559.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	ENSP00000512717.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000696560.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	ENSP00000512718.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000696561.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	ENSP00000512719.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000696562.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	ENSP00000512720.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000412585.7:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC MANE Select	ENSP00000399168.2:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000412585.6:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	ENSP00000399168.2:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
ENST00000481849.5:n.328+63_328+64insGGGGGGGGCCTGGGGGC
ENST00000497377.5:n.492+63_492+64insGGGGGGGGCCTGGGGGC
NM_005514.6:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	NP_005505.2:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
XM_011514556.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	XP_011512858.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
XM_011514557.1:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	XP_011512859.1:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
XR_926175.1:n.1532+63_1532+64insGGGGGGGGCCTGGGGGC
NM_005514.7:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC	NP_005505.2:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC
NM_005514.8:c.*4+63_*4+64insGGGGGGGGCCTGGGGGC MANE Select	NP_005505.2:n.*4+63_*4+64insGGGGGGGGCCTGGGGGC