Canonical Allele Identifier: CA513365391

Gene: TXNRD2

Linked Data

• COSMIC: COSM6161802 ; COSM6161803
• MyVariant Identifiers: chr22:g.19883051C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895528C>A , CM000684.2:g.19895528C>A	GRCh38
NC_000022.10:g.19883051C>A , CM000684.1:g.19883051C>A	GRCh37
NC_000022.9:g.18263051C>A	NCBI36
NG_011835.1:g.51309G>T , LRG_417:g.51309G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.828G>T MANE Select	ENSP00000383365.1:p.Leu276=
ENST00000334363.14:c.828G>T	ENSP00000334451.9:p.Leu276=
ENST00000400518.5:c.738G>T	ENSP00000383362.1:p.Leu246=
ENST00000400519.6:c.825G>T	ENSP00000383363.1:p.Leu275=
ENST00000400521.6:c.828G>T	ENSP00000383365.1:p.Leu276=
ENST00000400525.6:c.759G>T	ENSP00000383369.3:p.Leu253=
ENST00000474308.5:c.771G>T	ENSP00000485665.1:p.Leu257=
ENST00000475995.3:c.325G>T
ENST00000491939.6:c.732G>T	ENSP00000485543.1:p.Leu244=
ENST00000494454.5:n.902G>T
ENST00000542719.6:c.540G>T	ENSP00000485128.2:p.Leu180=
ENST00000634537.1:c.57G>T	ENSP00000489208.1:p.Leu19=
ENST00000635155.1:n.414G>T
NM_001282512.1:c.828G>T	NP_001269441.1:p.Leu276=
NM_006440.4:c.828G>T	NP_006431.2:p.Leu276=
NM_001282512.2:c.828G>T	NP_001269441.1:p.Leu276=
NM_001352300.1:c.825G>T	NP_001339229.1:p.Leu275=
NM_001352301.1:c.738G>T	NP_001339230.1:p.Leu246=
NM_001352302.1:c.540G>T	NP_001339231.1:p.Leu180=
NM_001352303.1:c.732G>T	NP_001339232.1:p.Leu244=
NR_147957.1:n.960G>T
NM_006440.5:c.828G>T MANE Select	NP_006431.2:p.Leu276=
NM_001282512.3:c.828G>T	NP_001269441.1:p.Leu276=
NM_001352300.2:c.825G>T	NP_001339229.1:p.Leu275=
NR_147957.2:n.786G>T
NM_001352301.2:c.738G>T	NP_001339230.1:p.Leu246=
NM_001352302.2:c.540G>T	NP_001339231.1:p.Leu180=
NM_001352303.2:c.732G>T	NP_001339232.1:p.Leu244=