Canonical Allele Identifier: CA8026315

Gene: ITGAX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31355958G>A , CM000678.2:g.31355958G>A	GRCh38
NC_000016.9:g.31367279G>A , CM000678.1:g.31367279G>A	GRCh37
NC_000016.8:g.31274780G>A	NCBI36
NG_011451.1:g.5771G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268296.9:c.103G>A MANE Select	ENSP00000268296.5:p.Ala35Thr
ENST00000268296.8:c.103G>A	ENSP00000268296.4:p.Ala35Thr
ENST00000562522.2:c.103G>A	ENSP00000454623.1:p.Ala35Thr
ENST00000562918.5:c.103G>A	ENSP00000483860.1:p.Ala35Thr
ENST00000564308.1:n.224G>A
ENST00000567409.1:n.170G>A
NM_000887.4:c.103G>A	NP_000878.2:p.Ala35Thr
NM_001286375.1:c.103G>A	NP_001273304.1:p.Ala35Thr
XM_011545852.1:c.103G>A	XP_011544154.1:p.Ala35Thr
XM_011545853.1:c.103G>A	XP_011544155.1:p.Ala35Thr
XM_011545854.1:c.103G>A	XP_011544156.1:p.Ala35Thr
XR_950797.1:n.191G>A
XR_950797.2:n.191G>A
NM_000887.5:c.103G>A MANE Select	NP_000878.2:p.Ala35Thr
NM_001286375.2:c.103G>A	NP_001273304.1:p.Ala35Thr