Canonical Allele Identifier: CA2839929063

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354423_31354424insGCCCCCCCCC , CM000668.2:g.31354423_31354424insGCCCCCCCCC	GRCh38
NC_000006.11:g.31322200_31322201insGCCCCCCCCC , CM000668.1:g.31322200_31322201insGCCCCCCCCC	GRCh37
NC_000006.10:g.31430179_31430180insGCCCCCCCCC	NCBI36
NG_023187.1:g.7789_7790insGGGGGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+55_3140+56insGGGGGGGGGC
ENST00000481849.6:n.3100+55_3100+56insGGGGGGGGGC
ENST00000497377.6:n.3007+55_3007+56insGGGGGGGGGC
ENST00000696558.1:c.1162+55_1162+56insGGGGGGGGGC	ENSP00000512716.1:n.1162+55_1162+56insGGGGGGGGGC
ENST00000696559.1:c.*4+55_*4+56insGGGGGGGGGC	ENSP00000512717.1:n.*4+55_*4+56insGGGGGGGGGC
ENST00000696560.1:c.*4+55_*4+56insGGGGGGGGGC	ENSP00000512718.1:n.*4+55_*4+56insGGGGGGGGGC
ENST00000696561.1:c.*4+55_*4+56insGGGGGGGGGC	ENSP00000512719.1:n.*4+55_*4+56insGGGGGGGGGC
ENST00000696562.1:c.*4+55_*4+56insGGGGGGGGGC	ENSP00000512720.1:n.*4+55_*4+56insGGGGGGGGGC
ENST00000412585.7:c.*4+55_*4+56insGGGGGGGGGC MANE Select	ENSP00000399168.2:n.*4+55_*4+56insGGGGGGGGGC
ENST00000412585.6:c.*4+55_*4+56insGGGGGGGGGC	ENSP00000399168.2:n.*4+55_*4+56insGGGGGGGGGC
ENST00000481849.5:n.328+55_328+56insGGGGGGGGGC
ENST00000497377.5:n.492+55_492+56insGGGGGGGGGC
NM_005514.6:c.*4+55_*4+56insGGGGGGGGGC	NP_005505.2:n.*4+55_*4+56insGGGGGGGGGC
XM_011514556.1:c.*4+55_*4+56insGGGGGGGGGC	XP_011512858.1:n.*4+55_*4+56insGGGGGGGGGC
XM_011514557.1:c.*4+55_*4+56insGGGGGGGGGC	XP_011512859.1:n.*4+55_*4+56insGGGGGGGGGC
XR_926175.1:n.1532+55_1532+56insGGGGGGGGGC
NM_005514.7:c.*4+55_*4+56insGGGGGGGGGC	NP_005505.2:n.*4+55_*4+56insGGGGGGGGGC
NM_005514.8:c.*4+55_*4+56insGGGGGGGGGC MANE Select	NP_005505.2:n.*4+55_*4+56insGGGGGGGGGC