Canonical Allele Identifier: CA2677954218

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354499-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354501_31354502insGCA , CM000668.2:g.31354501_31354502insGCA	GRCh38
NC_000006.11:g.31322278_31322279insGCA , CM000668.1:g.31322278_31322279insGCA	GRCh37
NC_000006.10:g.31430257_31430258insGCA	NCBI36
NG_023187.1:g.7713_7714insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3119_3120insCTG
ENST00000481849.6:n.3079_3080insCTG
ENST00000497377.6:n.2986_2987insCTG
ENST00000640094.2:c.955_956insCTG	ENSP00000491275.2:p.Asp318_Val319insAla
ENST00000696558.1:c.1141_1142insCTG	ENSP00000512716.1:n.1141_1142insCTG
ENST00000696559.1:c.1072_1073insCTG	ENSP00000512717.1:p.Asp357_Val358insAla
ENST00000696560.1:c.1072_1073insCTG	ENSP00000512718.1:p.Asp357_Val358insAla
ENST00000696561.1:c.1072_1073insCTG	ENSP00000512719.1:p.Asp357_Val358insAla
ENST00000696562.1:c.1072_1073insCTG	ENSP00000512720.1:p.Asp357_Val358insAla
ENST00000412585.7:c.1072_1073insCTG MANE Select	ENSP00000399168.2:p.Asp357_Val358insAla
ENST00000412585.6:c.1072_1073insCTG	ENSP00000399168.2:p.Asp357_Val358insAla
ENST00000481849.5:n.307_308insCTG
ENST00000497377.5:n.471_472insCTG
NM_005514.6:c.1072_1073insCTG	NP_005505.2:p.Asp357_Val358insAla
XM_011514556.1:c.1105_1106insCTG	XP_011512858.1:p.Asp368_Val369insAla
XM_011514557.1:c.955_956insCTG	XP_011512859.1:p.Asp318_Val319insAla
XR_926175.1:n.1511_1512insCTG
NM_005514.7:c.1072_1073insCTG	NP_005505.2:p.Asp357_Val358insAla
NM_005514.8:c.1072_1073insCTG MANE Select	NP_005505.2:p.Asp357_Val358insAla