Canonical Allele Identifier: CA2396103767

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918947A= , CM000684.2:g.19918947A=	GRCh38
NC_000022.10:g.19906470A= , CM000684.1:g.19906470A=	GRCh37
NC_000022.9:g.18286470A=	NCBI36
NG_011835.1:g.27890T= , LRG_417:g.27890T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.287T= MANE Select	ENSP00000383365.1:p.Leu96=
ENST00000334363.14:c.287T=	ENSP00000334451.9:p.Leu96=
ENST00000400518.5:c.197T=	ENSP00000383362.1:p.Leu66=
ENST00000400519.6:c.284T=	ENSP00000383363.1:p.Leu95=
ENST00000400521.6:c.287T=	ENSP00000383365.1:p.Leu96=
ENST00000400525.6:c.218T=	ENSP00000383369.3:p.Leu73=
ENST00000474308.5:c.230T=	ENSP00000485665.1:p.Leu77=
ENST00000491939.6:c.191T=	ENSP00000485543.1:p.Leu64=
ENST00000496729.2:n.292T=
ENST00000542719.6:c.-2T=	ENSP00000485128.2:n.-2T=
NM_001282512.1:c.287T=	NP_001269441.1:p.Leu96=
NM_006440.4:c.287T=	NP_006431.2:p.Leu96=
NM_001282512.2:c.287T=	NP_001269441.1:p.Leu96=
NM_001352300.1:c.284T=	NP_001339229.1:p.Leu95=
NM_001352301.1:c.197T=	NP_001339230.1:p.Leu66=
NM_001352302.1:c.-2T=	NP_001339231.1:n.-2T=
NM_001352303.1:c.191T=	NP_001339232.1:p.Leu64=
NR_147957.1:n.419T=
NM_006440.5:c.287T= MANE Select	NP_006431.2:p.Leu96=
NM_001282512.3:c.287T=	NP_001269441.1:p.Leu96=
NM_001352300.2:c.284T=	NP_001339229.1:p.Leu95=
NR_147957.2:n.245T=
NM_001352301.2:c.197T=	NP_001339230.1:p.Leu66=
NM_001352302.2:c.-2T=	NP_001339231.1:n.-2T=
NM_001352303.2:c.191T=	NP_001339232.1:p.Leu64=