Canonical Allele Identifier: CA2396084837

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880649C= , CM000684.2:g.19880649C=	GRCh38
NC_000022.10:g.19868172C= , CM000684.1:g.19868172C=	GRCh37
NC_000022.9:g.18248172C=	NCBI36
NG_011835.1:g.66188G= , LRG_417:g.66188G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1155G= MANE Select	ENSP00000383365.1:p.Gly385=
ENST00000400518.5:c.1065G=	ENSP00000383362.1:p.Gly355=
ENST00000400519.6:c.1152G=	ENSP00000383363.1:p.Gly384=
ENST00000400521.6:c.1155G=	ENSP00000383365.1:p.Gly385=
ENST00000400525.6:c.1086G=	ENSP00000383369.3:p.Gly362=
ENST00000462330.5:c.78G=	ENSP00000485603.2:p.Gly26=
ENST00000462843.2:c.105G=	ENSP00000485466.2:p.Gly35=
ENST00000474308.5:c.1098G=	ENSP00000485665.1:p.Gly366=
ENST00000485358.5:c.123G=	ENSP00000485499.2:p.Gly41=
ENST00000487165.5:n.1249G=
ENST00000494454.5:n.1229G=
ENST00000495655.2:n.699G=
ENST00000542719.6:c.867G=	ENSP00000485128.2:p.Gly289=
ENST00000634471.1:n.244-378G=
ENST00000634537.1:c.384G=	ENSP00000489208.1:p.Gly128=
NM_006440.4:c.1155G=	NP_006431.2:p.Gly385=
NM_001352300.1:c.1152G=	NP_001339229.1:p.Gly384=
NM_001352301.1:c.1065G=	NP_001339230.1:p.Gly355=
NM_001352302.1:c.867G=	NP_001339231.1:p.Gly289=
NR_147957.1:n.1287G=
NM_006440.5:c.1155G= MANE Select	NP_006431.2:p.Gly385=
NM_001352300.2:c.1152G=	NP_001339229.1:p.Gly384=
NR_147957.2:n.1113G=
NM_001352301.2:c.1065G=	NP_001339230.1:p.Gly355=
NM_001352302.2:c.867G=	NP_001339231.1:p.Gly289=