Canonical Allele Identifier: CA2396091884

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895293G= , CM000684.2:g.19895293G=	GRCh38
NC_000022.10:g.19882816G= , CM000684.1:g.19882816G=	GRCh37
NC_000022.9:g.18262816G=	NCBI36
NG_011835.1:g.51544C= , LRG_417:g.51544C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.949+114C= MANE Select	ENSP00000383365.1:n.949+114C=
ENST00000334363.14:c.950-93C=	ENSP00000334451.9:n.950-93C=
ENST00000400518.5:c.859+114C=	ENSP00000383362.1:n.859+114C=
ENST00000400519.6:c.946+114C=	ENSP00000383363.1:n.946+114C=
ENST00000400521.6:c.949+114C=	ENSP00000383365.1:n.949+114C=
ENST00000400525.6:c.880+114C=	ENSP00000383369.3:n.880+114C=
ENST00000474308.5:c.892+114C=	ENSP00000485665.1:n.892+114C=
ENST00000475995.3:c.474C=
ENST00000491939.6:c.854-93C=	ENSP00000485543.1:n.854-93C=
ENST00000494454.5:n.1023+114C=
ENST00000542719.6:c.661+114C=	ENSP00000485128.2:n.661+114C=
ENST00000634537.1:c.178+114C=	ENSP00000489208.1:n.178+114C=
ENST00000635155.1:n.535+114C=
NM_001282512.1:c.950-93C=	NP_001269441.1:n.950-93C=
NM_006440.4:c.949+114C=	NP_006431.2:n.949+114C=
NM_001282512.2:c.950-93C=	NP_001269441.1:n.950-93C=
NM_001352300.1:c.946+114C=	NP_001339229.1:n.946+114C=
NM_001352301.1:c.859+114C=	NP_001339230.1:n.859+114C=
NM_001352302.1:c.661+114C=	NP_001339231.1:n.661+114C=
NM_001352303.1:c.854-93C=	NP_001339232.1:n.854-93C=
NR_147957.1:n.1081+114C=
NM_006440.5:c.949+114C= MANE Select	NP_006431.2:n.949+114C=
NM_001282512.3:c.950-93C=	NP_001269441.1:n.950-93C=
NM_001352300.2:c.946+114C=	NP_001339229.1:n.946+114C=
NR_147957.2:n.907+114C=
NM_001352301.2:c.859+114C=	NP_001339230.1:n.859+114C=
NM_001352302.2:c.661+114C=	NP_001339231.1:n.661+114C=
NM_001352303.2:c.854-93C=	NP_001339232.1:n.854-93C=