Canonical Allele Identifier: CA2396084828

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880630A= , CM000684.2:g.19880630A=	GRCh38
NC_000022.10:g.19868153A= , CM000684.1:g.19868153A=	GRCh37
NC_000022.9:g.18248153A=	NCBI36
NG_011835.1:g.66207T= , LRG_417:g.66207T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1174T= MANE Select	ENSP00000383365.1:p.Tyr392=
ENST00000400518.5:c.1084T=	ENSP00000383362.1:p.Tyr362=
ENST00000400519.6:c.1171T=	ENSP00000383363.1:p.Tyr391=
ENST00000400521.6:c.1174T=	ENSP00000383365.1:p.Tyr392=
ENST00000400525.6:c.1105T=	ENSP00000383369.3:p.Tyr369=
ENST00000462330.5:c.97T=	ENSP00000485603.2:p.Tyr33=
ENST00000462843.2:c.124T=	ENSP00000485466.2:p.Tyr42=
ENST00000474308.5:c.1117T=	ENSP00000485665.1:p.Tyr373=
ENST00000485358.5:c.142T=	ENSP00000485499.2:p.Tyr48=
ENST00000487165.5:n.1268T=
ENST00000494454.5:n.1248T=
ENST00000495655.2:n.718T=
ENST00000542719.6:c.886T=	ENSP00000485128.2:p.Tyr296=
ENST00000634471.1:n.244-359T=
ENST00000634537.1:c.403T=	ENSP00000489208.1:p.Tyr135=
NM_006440.4:c.1174T=	NP_006431.2:p.Tyr392=
NM_001352300.1:c.1171T=	NP_001339229.1:p.Tyr391=
NM_001352301.1:c.1084T=	NP_001339230.1:p.Tyr362=
NM_001352302.1:c.886T=	NP_001339231.1:p.Tyr296=
NR_147957.1:n.1306T=
NM_006440.5:c.1174T= MANE Select	NP_006431.2:p.Tyr392=
NM_001352300.2:c.1171T=	NP_001339229.1:p.Tyr391=
NR_147957.2:n.1132T=
NM_001352301.2:c.1084T=	NP_001339230.1:p.Tyr362=
NM_001352302.2:c.886T=	NP_001339231.1:p.Tyr296=