Canonical Allele Identifier: CA2396105328

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19921847G= , CM000684.2:g.19921847G=	GRCh38
NC_000022.10:g.19909370G= , CM000684.1:g.19909370G=	GRCh37
NC_000022.9:g.18289370G=	NCBI36
NG_011835.1:g.24990C= , LRG_417:g.24990C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.173-2248C= MANE Select	ENSP00000383365.1:n.173-2248C=
ENST00000334363.14:c.173-2248C=	ENSP00000334451.9:n.173-2248C=
ENST00000400518.5:c.83-2248C=	ENSP00000383362.1:n.83-2248C=
ENST00000400519.6:c.170-2248C=	ENSP00000383363.1:n.170-2248C=
ENST00000400521.6:c.173-2248C=	ENSP00000383365.1:n.173-2248C=
ENST00000400525.6:c.104-2248C=	ENSP00000383369.3:n.104-2248C=
ENST00000474308.5:c.173-2843C=	ENSP00000485665.1:n.173-2843C=
ENST00000491939.6:c.77-2248C=	ENSP00000485543.1:n.77-2248C=
ENST00000496729.2:n.178-2248C=
ENST00000542719.6:c.-116-2248C=	ENSP00000485128.2:n.-116-2248C=
NM_001282512.1:c.173-2248C=	NP_001269441.1:n.173-2248C=
NM_006440.4:c.173-2248C=	NP_006431.2:n.173-2248C=
NM_001282512.2:c.173-2248C=	NP_001269441.1:n.173-2248C=
NM_001352300.1:c.170-2248C=	NP_001339229.1:n.170-2248C=
NM_001352301.1:c.83-2248C=	NP_001339230.1:n.83-2248C=
NM_001352302.1:c.-116-2248C=	NP_001339231.1:n.-116-2248C=
NM_001352303.1:c.77-2248C=	NP_001339232.1:n.77-2248C=
NR_147957.1:n.362-2843C=
NM_006440.5:c.173-2248C= MANE Select	NP_006431.2:n.173-2248C=
NM_001282512.3:c.173-2248C=	NP_001269441.1:n.173-2248C=
NM_001352300.2:c.170-2248C=	NP_001339229.1:n.170-2248C=
NR_147957.2:n.188-2843C=
NM_001352301.2:c.83-2248C=	NP_001339230.1:n.83-2248C=
NM_001352302.2:c.-116-2248C=	NP_001339231.1:n.-116-2248C=
NM_001352303.2:c.77-2248C=	NP_001339232.1:n.77-2248C=