Canonical Allele Identifier: CA10210847

Gene: TXN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36476826C>T , CM000684.2:g.36476826C>T	GRCh38
NC_000022.10:g.36872873C>T , CM000684.1:g.36872873C>T	GRCh37
NC_000022.9:g.35202819C>T	NCBI36
NG_046718.1:g.9815G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012473.4:c.294G>A MANE Select	NP_036605.2:p.Pro98=
ENST00000216185.7:c.294G>A MANE Select	ENSP00000216185.2:p.Pro98=
NM_012473.3:c.294G>A	NP_036605.2:p.Pro98=
ENST00000216185.6:c.294G>A	ENSP00000216185.2:p.Pro98=
ENST00000403313.5:c.294G>A	ENSP00000385393.1:p.Pro98=
ENST00000411915.1:c.294G>A	ENSP00000409407.1:p.Pro98=
ENST00000416967.1:c.-13G>A	ENSP00000469160.1:n.-13G>A
ENST00000487725.1:n.274G>A
XM_005261508.1:c.387G>A	XP_005261565.1:p.Pro129=
XM_006724226.1:c.294G>A	XP_006724289.1:p.Pro98=
XM_011530111.1:c.356+3749G>A	XP_011528413.1:n.356+3749G>A
XM_011530111.3:c.356+3749G>A	XP_011528413.1:n.356+3749G>A