Canonical Allele Identifier: CA2677953555

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354362-C-CTCACCACACATTCGAAACGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354362_31354363insTCACCACACATTCGAAACGT , CM000668.2:g.31354362_31354363insTCACCACACATTCGAAACGT	GRCh38
NC_000006.11:g.31322139_31322140insTCACCACACATTCGAAACGT , CM000668.1:g.31322139_31322140insTCACCACACATTCGAAACGT	GRCh37
NC_000006.10:g.31430118_31430119insTCACCACACATTCGAAACGT	NCBI36
NG_023187.1:g.7850_7851insACGTTTCGAATGTGTGGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3141-67_3141-66insACGTTTCGAATGTGTGGTGA
ENST00000481849.6:n.3101-67_3101-66insACGTTTCGAATGTGTGGTGA
ENST00000497377.6:n.3008-67_3008-66insACGTTTCGAATGTGTGGTGA
ENST00000696558.1:c.1163-67_1163-66insACGTTTCGAATGTGTGGTGA	ENSP00000512716.1:n.1163-67_1163-66insACGTTTCGAATGTGTGGTGA
ENST00000696559.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	ENSP00000512717.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000696560.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	ENSP00000512718.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000696561.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	ENSP00000512719.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000696562.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	ENSP00000512720.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000412585.7:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA MANE Select	ENSP00000399168.2:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000412585.6:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	ENSP00000399168.2:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
ENST00000481849.5:n.329-67_329-66insACGTTTCGAATGTGTGGTGA
ENST00000497377.5:n.493-67_493-66insACGTTTCGAATGTGTGGTGA
NM_005514.6:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	NP_005505.2:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
XM_011514556.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	XP_011512858.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
XM_011514557.1:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	XP_011512859.1:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
XR_926175.1:n.1533-67_1533-66insACGTTTCGAATGTGTGGTGA
NM_005514.7:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA	NP_005505.2:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA
NM_005514.8:c.*5-67_*5-66insACGTTTCGAATGTGTGGTGA MANE Select	NP_005505.2:n.*5-67_*5-66insACGTTTCGAATGTGTGGTGA