Canonical Allele Identifier: CA395720015

Gene: ITGAX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31355937A>G , CM000678.2:g.31355937A>G	GRCh38
NC_000016.9:g.31367258A>G , CM000678.1:g.31367258A>G	GRCh37
NC_000016.8:g.31274759A>G	NCBI36
NG_011451.1:g.5750A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268296.9:c.82A>G MANE Select	ENSP00000268296.5:p.Thr28Ala
ENST00000268296.8:c.82A>G	ENSP00000268296.4:p.Thr28Ala
ENST00000562522.2:c.82A>G	ENSP00000454623.1:p.Thr28Ala
ENST00000562918.5:c.82A>G	ENSP00000483860.1:p.Thr28Ala
ENST00000564308.1:n.203A>G
ENST00000567409.1:n.149A>G
NM_000887.4:c.82A>G	NP_000878.2:p.Thr28Ala
NM_001286375.1:c.82A>G	NP_001273304.1:p.Thr28Ala
XM_011545852.1:c.82A>G	XP_011544154.1:p.Thr28Ala
XM_011545853.1:c.82A>G	XP_011544155.1:p.Thr28Ala
XM_011545854.1:c.82A>G	XP_011544156.1:p.Thr28Ala
XR_950797.1:n.170A>G
XR_950797.2:n.170A>G
NM_000887.5:c.82A>G MANE Select	NP_000878.2:p.Thr28Ala
NM_001286375.2:c.82A>G	NP_001273304.1:p.Thr28Ala