Canonical Allele Identifier: CA513369116

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19906520C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918997C>G , CM000684.2:g.19918997C>G	GRCh38
NC_000022.10:g.19906520C>G , CM000684.1:g.19906520C>G	GRCh37
NC_000022.9:g.18286520C>G	NCBI36
NG_011835.1:g.27840G>C , LRG_417:g.27840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.237G>C MANE Select	ENSP00000383365.1:p.Arg79=
ENST00000334363.14:c.237G>C	ENSP00000334451.9:p.Arg79=
ENST00000400518.5:c.147G>C	ENSP00000383362.1:p.Arg49=
ENST00000400519.6:c.234G>C	ENSP00000383363.1:p.Arg78=
ENST00000400521.6:c.237G>C	ENSP00000383365.1:p.Arg79=
ENST00000400525.6:c.168G>C	ENSP00000383369.3:p.Arg56=
ENST00000474308.5:c.180G>C	ENSP00000485665.1:p.Arg60=
ENST00000491939.6:c.141G>C	ENSP00000485543.1:p.Arg47=
ENST00000496729.2:n.242G>C
ENST00000542719.6:c.-52G>C	ENSP00000485128.2:n.-52G>C
NM_001282512.1:c.237G>C	NP_001269441.1:p.Arg79=
NM_006440.4:c.237G>C	NP_006431.2:p.Arg79=
NM_001282512.2:c.237G>C	NP_001269441.1:p.Arg79=
NM_001352300.1:c.234G>C	NP_001339229.1:p.Arg78=
NM_001352301.1:c.147G>C	NP_001339230.1:p.Arg49=
NM_001352302.1:c.-52G>C	NP_001339231.1:n.-52G>C
NM_001352303.1:c.141G>C	NP_001339232.1:p.Arg47=
NR_147957.1:n.369G>C
NM_006440.5:c.237G>C MANE Select	NP_006431.2:p.Arg79=
NM_001282512.3:c.237G>C	NP_001269441.1:p.Arg79=
NM_001352300.2:c.234G>C	NP_001339229.1:p.Arg78=
NR_147957.2:n.195G>C
NM_001352301.2:c.147G>C	NP_001339230.1:p.Arg49=
NM_001352302.2:c.-52G>C	NP_001339231.1:n.-52G>C
NM_001352303.2:c.141G>C	NP_001339232.1:p.Arg47=