Canonical Allele Identifier: CA10210827

Gene: TXN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36476744T>C , CM000684.2:g.36476744T>C	GRCh38
NC_000022.10:g.36872791T>C , CM000684.1:g.36872791T>C	GRCh37
NC_000022.9:g.35202737T>C	NCBI36
NG_046718.1:g.9897A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216185.7:c.376A>G MANE Select	ENSP00000216185.2:p.Ile126Val
ENST00000216185.6:c.376A>G	ENSP00000216185.2:p.Ile126Val
ENST00000403313.5:c.376A>G	ENSP00000385393.1:p.Ile126Val
ENST00000411915.1:c.376A>G	ENSP00000409407.1:p.Ile126Val
ENST00000416967.1:c.70A>G	ENSP00000469160.1:p.Ile24Val
ENST00000487725.1:n.356A>G
NM_012473.3:c.376A>G	NP_036605.2:p.Ile126Val
XM_005261508.1:c.469A>G	XP_005261565.1:p.Ile157Val
XM_006724226.1:c.376A>G	XP_006724289.1:p.Ile126Val
XM_011530111.1:c.356+3831A>G	XP_011528413.1:n.356+3831A>G
XM_011530111.3:c.356+3831A>G	XP_011528413.1:n.356+3831A>G
NM_012473.4:c.376A>G MANE Select	NP_036605.2:p.Ile126Val