Canonical Allele Identifier: CA2396084859

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880679C= , CM000684.2:g.19880679C=	GRCh38
NC_000022.10:g.19868202C= , CM000684.1:g.19868202C=	GRCh37
NC_000022.9:g.18248202C=	NCBI36
NG_011835.1:g.66158G= , LRG_417:g.66158G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1125G= MANE Select	ENSP00000383365.1:p.Gly375=
ENST00000400518.5:c.1035G=	ENSP00000383362.1:p.Gly345=
ENST00000400519.6:c.1122G=	ENSP00000383363.1:p.Gly374=
ENST00000400521.6:c.1125G=	ENSP00000383365.1:p.Gly375=
ENST00000400525.6:c.1056G=	ENSP00000383369.3:p.Gly352=
ENST00000462330.5:c.48G=	ENSP00000485603.2:p.Gly16=
ENST00000462843.2:c.75G=	ENSP00000485466.2:p.Gly25=
ENST00000474308.5:c.1068G=	ENSP00000485665.1:p.Gly356=
ENST00000485358.5:c.93G=	ENSP00000485499.2:p.Gly31=
ENST00000487165.5:n.1219G=
ENST00000494454.5:n.1199G=
ENST00000495655.2:n.669G=
ENST00000542719.6:c.837G=	ENSP00000485128.2:p.Gly279=
ENST00000634471.1:n.244-408G=
ENST00000634537.1:c.354G=	ENSP00000489208.1:p.Gly118=
NM_006440.4:c.1125G=	NP_006431.2:p.Gly375=
NM_001352300.1:c.1122G=	NP_001339229.1:p.Gly374=
NM_001352301.1:c.1035G=	NP_001339230.1:p.Gly345=
NM_001352302.1:c.837G=	NP_001339231.1:p.Gly279=
NR_147957.1:n.1257G=
NM_006440.5:c.1125G= MANE Select	NP_006431.2:p.Gly375=
NM_001352300.2:c.1122G=	NP_001339229.1:p.Gly374=
NR_147957.2:n.1083G=
NM_001352301.2:c.1035G=	NP_001339230.1:p.Gly345=
NM_001352302.2:c.837G=	NP_001339231.1:p.Gly279=