Canonical Allele Identifier: CA2396084826

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880628G= , CM000684.2:g.19880628G=	GRCh38
NC_000022.10:g.19868151G= , CM000684.1:g.19868151G=	GRCh37
NC_000022.9:g.18248151G=	NCBI36
NG_011835.1:g.66209C= , LRG_417:g.66209C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1176C= MANE Select	ENSP00000383365.1:p.Tyr392=
ENST00000400518.5:c.1086C=	ENSP00000383362.1:p.Tyr362=
ENST00000400519.6:c.1173C=	ENSP00000383363.1:p.Tyr391=
ENST00000400521.6:c.1176C=	ENSP00000383365.1:p.Tyr392=
ENST00000400525.6:c.1107C=	ENSP00000383369.3:p.Tyr369=
ENST00000462330.5:c.99C=	ENSP00000485603.2:p.Tyr33=
ENST00000462843.2:c.126C=	ENSP00000485466.2:p.Tyr42=
ENST00000474308.5:c.1119C=	ENSP00000485665.1:p.Tyr373=
ENST00000485358.5:c.144C=	ENSP00000485499.2:p.Tyr48=
ENST00000487165.5:n.1270C=
ENST00000494454.5:n.1250C=
ENST00000495655.2:n.720C=
ENST00000542719.6:c.888C=	ENSP00000485128.2:p.Tyr296=
ENST00000634471.1:n.244-357C=
ENST00000634537.1:c.405C=	ENSP00000489208.1:p.Tyr135=
NM_006440.4:c.1176C=	NP_006431.2:p.Tyr392=
NM_001352300.1:c.1173C=	NP_001339229.1:p.Tyr391=
NM_001352301.1:c.1086C=	NP_001339230.1:p.Tyr362=
NM_001352302.1:c.888C=	NP_001339231.1:p.Tyr296=
NR_147957.1:n.1308C=
NM_006440.5:c.1176C= MANE Select	NP_006431.2:p.Tyr392=
NM_001352300.2:c.1173C=	NP_001339229.1:p.Tyr391=
NR_147957.2:n.1134C=
NM_001352301.2:c.1086C=	NP_001339230.1:p.Tyr362=
NM_001352302.2:c.888C=	NP_001339231.1:p.Tyr296=