Canonical Allele Identifier: CA2396103727

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918877C= , CM000684.2:g.19918877C=	GRCh38
NC_000022.10:g.19906400C= , CM000684.1:g.19906400C=	GRCh37
NC_000022.9:g.18286400C=	NCBI36
NG_011835.1:g.27960G= , LRG_417:g.27960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.357G= MANE Select	ENSP00000383365.1:p.Gln119=
ENST00000334363.14:c.357G=	ENSP00000334451.9:p.Gln119=
ENST00000400518.5:c.267G=	ENSP00000383362.1:p.Gln89=
ENST00000400519.6:c.354G=	ENSP00000383363.1:p.Gln118=
ENST00000400521.6:c.357G=	ENSP00000383365.1:p.Gln119=
ENST00000400525.6:c.288G=	ENSP00000383369.3:p.Gln96=
ENST00000474308.5:c.300G=	ENSP00000485665.1:p.Gln100=
ENST00000491939.6:c.261G=	ENSP00000485543.1:p.Gln87=
ENST00000496729.2:n.362G=
ENST00000542719.6:c.69G=	ENSP00000485128.2:p.Gln23=
NM_001282512.1:c.357G=	NP_001269441.1:p.Gln119=
NM_006440.4:c.357G=	NP_006431.2:p.Gln119=
NM_001282512.2:c.357G=	NP_001269441.1:p.Gln119=
NM_001352300.1:c.354G=	NP_001339229.1:p.Gln118=
NM_001352301.1:c.267G=	NP_001339230.1:p.Gln89=
NM_001352302.1:c.69G=	NP_001339231.1:p.Gln23=
NM_001352303.1:c.261G=	NP_001339232.1:p.Gln87=
NR_147957.1:n.489G=
NM_006440.5:c.357G= MANE Select	NP_006431.2:p.Gln119=
NM_001282512.3:c.357G=	NP_001269441.1:p.Gln119=
NM_001352300.2:c.354G=	NP_001339229.1:p.Gln118=
NR_147957.2:n.315G=
NM_001352301.2:c.267G=	NP_001339230.1:p.Gln89=
NM_001352302.2:c.69G=	NP_001339231.1:p.Gln23=
NM_001352303.2:c.261G=	NP_001339232.1:p.Gln87=