Canonical Allele Identifier: CA2396103724

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918873C= , CM000684.2:g.19918873C=	GRCh38
NC_000022.10:g.19906396C= , CM000684.1:g.19906396C=	GRCh37
NC_000022.9:g.18286396C=	NCBI36
NG_011835.1:g.27964G= , LRG_417:g.27964G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.361G= MANE Select	ENSP00000383365.1:p.Val121=
ENST00000334363.14:c.361G=	ENSP00000334451.9:p.Val121=
ENST00000400518.5:c.271G=	ENSP00000383362.1:p.Val91=
ENST00000400519.6:c.358G=	ENSP00000383363.1:p.Val120=
ENST00000400521.6:c.361G=	ENSP00000383365.1:p.Val121=
ENST00000400525.6:c.292G=	ENSP00000383369.3:p.Val98=
ENST00000474308.5:c.304G=	ENSP00000485665.1:p.Val102=
ENST00000491939.6:c.265G=	ENSP00000485543.1:p.Val89=
ENST00000496729.2:n.366G=
ENST00000542719.6:c.73G=	ENSP00000485128.2:p.Val25=
NM_001282512.1:c.361G=	NP_001269441.1:p.Val121=
NM_006440.4:c.361G=	NP_006431.2:p.Val121=
NM_001282512.2:c.361G=	NP_001269441.1:p.Val121=
NM_001352300.1:c.358G=	NP_001339229.1:p.Val120=
NM_001352301.1:c.271G=	NP_001339230.1:p.Val91=
NM_001352302.1:c.73G=	NP_001339231.1:p.Val25=
NM_001352303.1:c.265G=	NP_001339232.1:p.Val89=
NR_147957.1:n.493G=
NM_006440.5:c.361G= MANE Select	NP_006431.2:p.Val121=
NM_001282512.3:c.361G=	NP_001269441.1:p.Val121=
NM_001352300.2:c.358G=	NP_001339229.1:p.Val120=
NR_147957.2:n.319G=
NM_001352301.2:c.271G=	NP_001339230.1:p.Val91=
NM_001352302.2:c.73G=	NP_001339231.1:p.Val25=
NM_001352303.2:c.265G=	NP_001339232.1:p.Val89=