Canonical Allele Identifier: CA2840254779

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354422_31354423insTCCCC , CM000668.2:g.31354422_31354423insTCCCC	GRCh38
NC_000006.11:g.31322199_31322200insTCCCC , CM000668.1:g.31322199_31322200insTCCCC	GRCh37
NC_000006.10:g.31430178_31430179insTCCCC	NCBI36
NG_023187.1:g.7790_7791insGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+56_3140+57insGGGGA
ENST00000481849.6:n.3100+56_3100+57insGGGGA
ENST00000497377.6:n.3007+56_3007+57insGGGGA
ENST00000696558.1:c.1162+56_1162+57insGGGGA	ENSP00000512716.1:n.1162+56_1162+57insGGGGA
ENST00000696559.1:c.*4+56_*4+57insGGGGA	ENSP00000512717.1:n.*4+56_*4+57insGGGGA
ENST00000696560.1:c.*4+56_*4+57insGGGGA	ENSP00000512718.1:n.*4+56_*4+57insGGGGA
ENST00000696561.1:c.*4+56_*4+57insGGGGA	ENSP00000512719.1:n.*4+56_*4+57insGGGGA
ENST00000696562.1:c.*4+56_*4+57insGGGGA	ENSP00000512720.1:n.*4+56_*4+57insGGGGA
ENST00000412585.7:c.*4+56_*4+57insGGGGA MANE Select	ENSP00000399168.2:n.*4+56_*4+57insGGGGA
ENST00000412585.6:c.*4+56_*4+57insGGGGA	ENSP00000399168.2:n.*4+56_*4+57insGGGGA
ENST00000481849.5:n.328+56_328+57insGGGGA
ENST00000497377.5:n.492+56_492+57insGGGGA
NM_005514.6:c.*4+56_*4+57insGGGGA	NP_005505.2:n.*4+56_*4+57insGGGGA
XM_011514556.1:c.*4+56_*4+57insGGGGA	XP_011512858.1:n.*4+56_*4+57insGGGGA
XM_011514557.1:c.*4+56_*4+57insGGGGA	XP_011512859.1:n.*4+56_*4+57insGGGGA
XR_926175.1:n.1532+56_1532+57insGGGGA
NM_005514.7:c.*4+56_*4+57insGGGGA	NP_005505.2:n.*4+56_*4+57insGGGGA
NM_005514.8:c.*4+56_*4+57insGGGGA MANE Select	NP_005505.2:n.*4+56_*4+57insGGGGA