Canonical Allele Identifier: CA2396103877

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919153C= , CM000684.2:g.19919153C=	GRCh38
NC_000022.10:g.19906676C= , CM000684.1:g.19906676C=	GRCh37
NC_000022.9:g.18286676C=	NCBI36
NG_011835.1:g.27684G= , LRG_417:g.27684G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.230-149G= MANE Select	ENSP00000383365.1:n.230-149G=
ENST00000334363.14:c.230-149G=	ENSP00000334451.9:n.230-149G=
ENST00000400518.5:c.140-149G=	ENSP00000383362.1:n.140-149G=
ENST00000400519.6:c.227-149G=	ENSP00000383363.1:n.227-149G=
ENST00000400521.6:c.230-149G=	ENSP00000383365.1:n.230-149G=
ENST00000400525.6:c.161-149G=	ENSP00000383369.3:n.161-149G=
ENST00000474308.5:c.173-149G=	ENSP00000485665.1:n.173-149G=
ENST00000491939.6:c.134-149G=	ENSP00000485543.1:n.134-149G=
ENST00000496729.2:n.235-149G=
ENST00000542719.6:c.-59-149G=	ENSP00000485128.2:n.-59-149G=
NM_001282512.1:c.230-149G=	NP_001269441.1:n.230-149G=
NM_006440.4:c.230-149G=	NP_006431.2:n.230-149G=
NM_001282512.2:c.230-149G=	NP_001269441.1:n.230-149G=
NM_001352300.1:c.227-149G=	NP_001339229.1:n.227-149G=
NM_001352301.1:c.140-149G=	NP_001339230.1:n.140-149G=
NM_001352302.1:c.-59-149G=	NP_001339231.1:n.-59-149G=
NM_001352303.1:c.134-149G=	NP_001339232.1:n.134-149G=
NR_147957.1:n.362-149G=
NM_006440.5:c.230-149G= MANE Select	NP_006431.2:n.230-149G=
NM_001282512.3:c.230-149G=	NP_001269441.1:n.230-149G=
NM_001352300.2:c.227-149G=	NP_001339229.1:n.227-149G=
NR_147957.2:n.188-149G=
NM_001352301.2:c.140-149G=	NP_001339230.1:n.140-149G=
NM_001352302.2:c.-59-149G=	NP_001339231.1:n.-59-149G=
NM_001352303.2:c.134-149G=	NP_001339232.1:n.134-149G=