Canonical Allele Identifier: CA2396103783

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918973G= , CM000684.2:g.19918973G=	GRCh38
NC_000022.10:g.19906496G= , CM000684.1:g.19906496G=	GRCh37
NC_000022.9:g.18286496G=	NCBI36
NG_011835.1:g.27864C= , LRG_417:g.27864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.261C= MANE Select	ENSP00000383365.1:p.Val87=
ENST00000334363.14:c.261C=	ENSP00000334451.9:p.Val87=
ENST00000400518.5:c.171C=	ENSP00000383362.1:p.Val57=
ENST00000400519.6:c.258C=	ENSP00000383363.1:p.Val86=
ENST00000400521.6:c.261C=	ENSP00000383365.1:p.Val87=
ENST00000400525.6:c.192C=	ENSP00000383369.3:p.Val64=
ENST00000474308.5:c.204C=	ENSP00000485665.1:p.Val68=
ENST00000491939.6:c.165C=	ENSP00000485543.1:p.Val55=
ENST00000496729.2:n.266C=
ENST00000542719.6:c.-28C=	ENSP00000485128.2:n.-28C=
NM_001282512.1:c.261C=	NP_001269441.1:p.Val87=
NM_006440.4:c.261C=	NP_006431.2:p.Val87=
NM_001282512.2:c.261C=	NP_001269441.1:p.Val87=
NM_001352300.1:c.258C=	NP_001339229.1:p.Val86=
NM_001352301.1:c.171C=	NP_001339230.1:p.Val57=
NM_001352302.1:c.-28C=	NP_001339231.1:n.-28C=
NM_001352303.1:c.165C=	NP_001339232.1:p.Val55=
NR_147957.1:n.393C=
NM_006440.5:c.261C= MANE Select	NP_006431.2:p.Val87=
NM_001282512.3:c.261C=	NP_001269441.1:p.Val87=
NM_001352300.2:c.258C=	NP_001339229.1:p.Val86=
NR_147957.2:n.219C=
NM_001352301.2:c.171C=	NP_001339230.1:p.Val57=
NM_001352302.2:c.-28C=	NP_001339231.1:n.-28C=
NM_001352303.2:c.165C=	NP_001339232.1:p.Val55=