Canonical Allele Identifier: CA2396103906

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919201A= , CM000684.2:g.19919201A=	GRCh38
NC_000022.10:g.19906724A= , CM000684.1:g.19906724A=	GRCh37
NC_000022.9:g.18286724A=	NCBI36
NG_011835.1:g.27636T= , LRG_417:g.27636T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.230-197T= MANE Select	ENSP00000383365.1:n.230-197T=
ENST00000334363.14:c.230-197T=	ENSP00000334451.9:n.230-197T=
ENST00000400518.5:c.140-197T=	ENSP00000383362.1:n.140-197T=
ENST00000400519.6:c.227-197T=	ENSP00000383363.1:n.227-197T=
ENST00000400521.6:c.230-197T=	ENSP00000383365.1:n.230-197T=
ENST00000400525.6:c.161-197T=	ENSP00000383369.3:n.161-197T=
ENST00000474308.5:c.173-197T=	ENSP00000485665.1:n.173-197T=
ENST00000491939.6:c.134-197T=	ENSP00000485543.1:n.134-197T=
ENST00000496729.2:n.235-197T=
ENST00000542719.6:c.-59-197T=	ENSP00000485128.2:n.-59-197T=
NM_001282512.1:c.230-197T=	NP_001269441.1:n.230-197T=
NM_006440.4:c.230-197T=	NP_006431.2:n.230-197T=
NM_001282512.2:c.230-197T=	NP_001269441.1:n.230-197T=
NM_001352300.1:c.227-197T=	NP_001339229.1:n.227-197T=
NM_001352301.1:c.140-197T=	NP_001339230.1:n.140-197T=
NM_001352302.1:c.-59-197T=	NP_001339231.1:n.-59-197T=
NM_001352303.1:c.134-197T=	NP_001339232.1:n.134-197T=
NR_147957.1:n.362-197T=
NM_006440.5:c.230-197T= MANE Select	NP_006431.2:n.230-197T=
NM_001282512.3:c.230-197T=	NP_001269441.1:n.230-197T=
NM_001352300.2:c.227-197T=	NP_001339229.1:n.227-197T=
NR_147957.2:n.188-197T=
NM_001352301.2:c.140-197T=	NP_001339230.1:n.140-197T=
NM_001352302.2:c.-59-197T=	NP_001339231.1:n.-59-197T=
NM_001352303.2:c.134-197T=	NP_001339232.1:n.134-197T=