Canonical Allele Identifier: CA2403887518

Gene: TXN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36476703T= , CM000684.2:g.36476703T=	GRCh38
NC_000022.10:g.36872750T= , CM000684.1:g.36872750T=	GRCh37
NC_000022.9:g.35202696T=	NCBI36
NG_046718.1:g.9938A=

Transcript Alleles

HGVS	Amino-acid Change
NM_012473.4:c.387+30A= MANE Select	NP_036605.2:n.387+30A=
ENST00000216185.7:c.387+30A= MANE Select	ENSP00000216185.2:n.387+30A=
NM_012473.3:c.387+30A=	NP_036605.2:n.387+30A=
ENST00000216185.6:c.387+30A=	ENSP00000216185.2:n.387+30A=
ENST00000403313.5:c.387+30A=	ENSP00000385393.1:n.387+30A=
ENST00000411915.1:c.387+30A=	ENSP00000409407.1:n.387+30A=
ENST00000416967.1:c.81+30A=	ENSP00000469160.1:n.81+30A=
ENST00000487725.1:n.367+30A=
XM_005261508.1:c.480+30A=	XP_005261565.1:n.480+30A=
XM_006724226.1:c.387+30A=	XP_006724289.1:n.387+30A=
XM_011530111.1:c.356+3872A=	XP_011528413.1:n.356+3872A=
XM_011530111.3:c.356+3872A=	XP_011528413.1:n.356+3872A=