Canonical Allele Identifier: CA2396084827

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880629T= , CM000684.2:g.19880629T=	GRCh38
NC_000022.10:g.19868152T= , CM000684.1:g.19868152T=	GRCh37
NC_000022.9:g.18248152T=	NCBI36
NG_011835.1:g.66208A= , LRG_417:g.66208A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1175A= MANE Select	ENSP00000383365.1:p.Tyr392=
ENST00000400518.5:c.1085A=	ENSP00000383362.1:p.Tyr362=
ENST00000400519.6:c.1172A=	ENSP00000383363.1:p.Tyr391=
ENST00000400521.6:c.1175A=	ENSP00000383365.1:p.Tyr392=
ENST00000400525.6:c.1106A=	ENSP00000383369.3:p.Tyr369=
ENST00000462330.5:c.98A=	ENSP00000485603.2:p.Tyr33=
ENST00000462843.2:c.125A=	ENSP00000485466.2:p.Tyr42=
ENST00000474308.5:c.1118A=	ENSP00000485665.1:p.Tyr373=
ENST00000485358.5:c.143A=	ENSP00000485499.2:p.Tyr48=
ENST00000487165.5:n.1269A=
ENST00000494454.5:n.1249A=
ENST00000495655.2:n.719A=
ENST00000542719.6:c.887A=	ENSP00000485128.2:p.Tyr296=
ENST00000634471.1:n.244-358A=
ENST00000634537.1:c.404A=	ENSP00000489208.1:p.Tyr135=
NM_006440.4:c.1175A=	NP_006431.2:p.Tyr392=
NM_001352300.1:c.1172A=	NP_001339229.1:p.Tyr391=
NM_001352301.1:c.1085A=	NP_001339230.1:p.Tyr362=
NM_001352302.1:c.887A=	NP_001339231.1:p.Tyr296=
NR_147957.1:n.1307A=
NM_006440.5:c.1175A= MANE Select	NP_006431.2:p.Tyr392=
NM_001352300.2:c.1172A=	NP_001339229.1:p.Tyr391=
NR_147957.2:n.1133A=
NM_001352301.2:c.1085A=	NP_001339230.1:p.Tyr362=
NM_001352302.2:c.887A=	NP_001339231.1:p.Tyr296=