Canonical Allele Identifier: CA2396103726

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918876G= , CM000684.2:g.19918876G=	GRCh38
NC_000022.10:g.19906399G= , CM000684.1:g.19906399G=	GRCh37
NC_000022.9:g.18286399G=	NCBI36
NG_011835.1:g.27961C= , LRG_417:g.27961C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.358C= MANE Select	ENSP00000383365.1:p.Pro120=
ENST00000334363.14:c.358C=	ENSP00000334451.9:p.Pro120=
ENST00000400518.5:c.268C=	ENSP00000383362.1:p.Pro90=
ENST00000400519.6:c.355C=	ENSP00000383363.1:p.Pro119=
ENST00000400521.6:c.358C=	ENSP00000383365.1:p.Pro120=
ENST00000400525.6:c.289C=	ENSP00000383369.3:p.Pro97=
ENST00000474308.5:c.301C=	ENSP00000485665.1:p.Pro101=
ENST00000491939.6:c.262C=	ENSP00000485543.1:p.Pro88=
ENST00000496729.2:n.363C=
ENST00000542719.6:c.70C=	ENSP00000485128.2:p.Pro24=
NM_001282512.1:c.358C=	NP_001269441.1:p.Pro120=
NM_006440.4:c.358C=	NP_006431.2:p.Pro120=
NM_001282512.2:c.358C=	NP_001269441.1:p.Pro120=
NM_001352300.1:c.355C=	NP_001339229.1:p.Pro119=
NM_001352301.1:c.268C=	NP_001339230.1:p.Pro90=
NM_001352302.1:c.70C=	NP_001339231.1:p.Pro24=
NM_001352303.1:c.262C=	NP_001339232.1:p.Pro88=
NR_147957.1:n.490C=
NM_006440.5:c.358C= MANE Select	NP_006431.2:p.Pro120=
NM_001282512.3:c.358C=	NP_001269441.1:p.Pro120=
NM_001352300.2:c.355C=	NP_001339229.1:p.Pro119=
NR_147957.2:n.316C=
NM_001352301.2:c.268C=	NP_001339230.1:p.Pro90=
NM_001352302.2:c.70C=	NP_001339231.1:p.Pro24=
NM_001352303.2:c.262C=	NP_001339232.1:p.Pro88=