Canonical Allele Identifier: CA10103857

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19883375G>A , CM000684.2:g.19883375G>A	GRCh38
NC_000022.10:g.19870898G>A , CM000684.1:g.19870898G>A	GRCh37
NC_000022.9:g.18250898G>A	NCBI36
NG_011835.1:g.63462C>T , LRG_417:g.63462C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.1036C>T MANE Select	NP_006431.2:p.Arg346Trp
ENST00000400521.7:c.1036C>T MANE Select	ENSP00000383365.1:p.Arg346Trp
NM_001352300.1:c.1033C>T	NP_001339229.1:p.Arg345Trp
NM_001352300.2:c.1033C>T	NP_001339229.1:p.Arg345Trp
NM_001352301.1:c.946C>T	NP_001339230.1:p.Arg316Trp
NM_001352301.2:c.946C>T	NP_001339230.1:p.Arg316Trp
NM_001352302.1:c.748C>T	NP_001339231.1:p.Arg250Trp
NM_001352302.2:c.748C>T	NP_001339231.1:p.Arg250Trp
NM_006440.4:c.1036C>T	NP_006431.2:p.Arg346Trp
NR_147957.1:n.1168C>T
NR_147957.2:n.994C>T
ENST00000400518.5:c.946C>T	ENSP00000383362.1:p.Arg316Trp
ENST00000400519.6:c.1033C>T	ENSP00000383363.1:p.Arg345Trp
ENST00000400521.6:c.1036C>T	ENSP00000383365.1:p.Arg346Trp
ENST00000400525.6:c.967C>T	ENSP00000383369.3:p.Arg323Trp
ENST00000474308.5:c.979C>T	ENSP00000485665.1:p.Arg327Trp
ENST00000487165.5:n.1130C>T
ENST00000494454.5:n.1110C>T
ENST00000542719.6:c.748C>T	ENSP00000485128.2:p.Arg250Trp
ENST00000634471.1:n.193C>T
ENST00000634537.1:c.265C>T	ENSP00000489208.1:p.Arg89Trp