Canonical Allele Identifier: CA2396092038

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895623G= , CM000684.2:g.19895623G=	GRCh38
NC_000022.10:g.19883146G= , CM000684.1:g.19883146G=	GRCh37
NC_000022.9:g.18263146G=	NCBI36
NG_011835.1:g.51214C= , LRG_417:g.51214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.775-42C= MANE Select	ENSP00000383365.1:n.775-42C=
ENST00000334363.14:c.775-42C=	ENSP00000334451.9:n.775-42C=
ENST00000400518.5:c.685-42C=	ENSP00000383362.1:n.685-42C=
ENST00000400519.6:c.772-42C=	ENSP00000383363.1:n.772-42C=
ENST00000400521.6:c.775-42C=	ENSP00000383365.1:n.775-42C=
ENST00000400525.6:c.706-42C=	ENSP00000383369.3:n.706-42C=
ENST00000474308.5:c.718-42C=	ENSP00000485665.1:n.718-42C=
ENST00000475995.3:c.272-42C=
ENST00000491939.6:c.679-42C=	ENSP00000485543.1:n.679-42C=
ENST00000494454.5:n.849-42C=
ENST00000542719.6:c.487-42C=	ENSP00000485128.2:n.487-42C=
ENST00000634537.1:c.4-42C=	ENSP00000489208.1:n.4-42C=
ENST00000635155.1:n.361-42C=
NM_001282512.1:c.775-42C=	NP_001269441.1:n.775-42C=
NM_006440.4:c.775-42C=	NP_006431.2:n.775-42C=
NM_001282512.2:c.775-42C=	NP_001269441.1:n.775-42C=
NM_001352300.1:c.772-42C=	NP_001339229.1:n.772-42C=
NM_001352301.1:c.685-42C=	NP_001339230.1:n.685-42C=
NM_001352302.1:c.487-42C=	NP_001339231.1:n.487-42C=
NM_001352303.1:c.679-42C=	NP_001339232.1:n.679-42C=
NR_147957.1:n.907-42C=
NM_006440.5:c.775-42C= MANE Select	NP_006431.2:n.775-42C=
NM_001282512.3:c.775-42C=	NP_001269441.1:n.775-42C=
NM_001352300.2:c.772-42C=	NP_001339229.1:n.772-42C=
NR_147957.2:n.733-42C=
NM_001352301.2:c.685-42C=	NP_001339230.1:n.685-42C=
NM_001352302.2:c.487-42C=	NP_001339231.1:n.487-42C=
NM_001352303.2:c.679-42C=	NP_001339232.1:n.679-42C=