Canonical Allele Identifier: CA2396091962

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895451C= , CM000684.2:g.19895451C=	GRCh38
NC_000022.10:g.19882974C= , CM000684.1:g.19882974C=	GRCh37
NC_000022.9:g.18262974C=	NCBI36
NG_011835.1:g.51386G= , LRG_417:g.51386G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.905G= MANE Select	ENSP00000383365.1:p.Gly302=
ENST00000334363.14:c.905G=	ENSP00000334451.9:p.Gly302=
ENST00000400518.5:c.815G=	ENSP00000383362.1:p.Gly272=
ENST00000400519.6:c.902G=	ENSP00000383363.1:p.Gly301=
ENST00000400521.6:c.905G=	ENSP00000383365.1:p.Gly302=
ENST00000400525.6:c.836G=	ENSP00000383369.3:p.Gly279=
ENST00000474308.5:c.848G=	ENSP00000485665.1:p.Gly283=
ENST00000475995.3:c.402G=
ENST00000491939.6:c.809G=	ENSP00000485543.1:p.Gly270=
ENST00000494454.5:n.979G=
ENST00000542719.6:c.617G=	ENSP00000485128.2:p.Gly206=
ENST00000634537.1:c.134G=	ENSP00000489208.1:p.Gly45=
ENST00000635155.1:n.491G=
NM_001282512.1:c.905G=	NP_001269441.1:p.Gly302=
NM_006440.4:c.905G=	NP_006431.2:p.Gly302=
NM_001282512.2:c.905G=	NP_001269441.1:p.Gly302=
NM_001352300.1:c.902G=	NP_001339229.1:p.Gly301=
NM_001352301.1:c.815G=	NP_001339230.1:p.Gly272=
NM_001352302.1:c.617G=	NP_001339231.1:p.Gly206=
NM_001352303.1:c.809G=	NP_001339232.1:p.Gly270=
NR_147957.1:n.1037G=
NM_006440.5:c.905G= MANE Select	NP_006431.2:p.Gly302=
NM_001282512.3:c.905G=	NP_001269441.1:p.Gly302=
NM_001352300.2:c.902G=	NP_001339229.1:p.Gly301=
NR_147957.2:n.863G=
NM_001352301.2:c.815G=	NP_001339230.1:p.Gly272=
NM_001352302.2:c.617G=	NP_001339231.1:p.Gly206=
NM_001352303.2:c.809G=	NP_001339232.1:p.Gly270=