Canonical Allele Identifier: CA2396103610

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918649G= , CM000684.2:g.19918649G=	GRCh38
NC_000022.10:g.19906172G= , CM000684.1:g.19906172G=	GRCh37
NC_000022.9:g.18286172G=	NCBI36
NG_011835.1:g.28188C= , LRG_417:g.28188C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.374+211C= MANE Select	ENSP00000383365.1:n.374+211C=
ENST00000334363.14:c.374+211C=	ENSP00000334451.9:n.374+211C=
ENST00000400518.5:c.284+211C=	ENSP00000383362.1:n.284+211C=
ENST00000400519.6:c.371+211C=	ENSP00000383363.1:n.371+211C=
ENST00000400521.6:c.374+211C=	ENSP00000383365.1:n.374+211C=
ENST00000400525.6:c.305+211C=	ENSP00000383369.3:n.305+211C=
ENST00000474308.5:c.317+211C=	ENSP00000485665.1:n.317+211C=
ENST00000491939.6:c.278+211C=	ENSP00000485543.1:n.278+211C=
ENST00000496729.2:n.379+211C=
ENST00000542719.6:c.86+211C=	ENSP00000485128.2:n.86+211C=
NM_001282512.1:c.374+211C=	NP_001269441.1:n.374+211C=
NM_006440.4:c.374+211C=	NP_006431.2:n.374+211C=
NM_001282512.2:c.374+211C=	NP_001269441.1:n.374+211C=
NM_001352300.1:c.371+211C=	NP_001339229.1:n.371+211C=
NM_001352301.1:c.284+211C=	NP_001339230.1:n.284+211C=
NM_001352302.1:c.86+211C=	NP_001339231.1:n.86+211C=
NM_001352303.1:c.278+211C=	NP_001339232.1:n.278+211C=
NR_147957.1:n.506+211C=
NM_006440.5:c.374+211C= MANE Select	NP_006431.2:n.374+211C=
NM_001282512.3:c.374+211C=	NP_001269441.1:n.374+211C=
NM_001352300.2:c.371+211C=	NP_001339229.1:n.371+211C=
NR_147957.2:n.332+211C=
NM_001352301.2:c.284+211C=	NP_001339230.1:n.284+211C=
NM_001352302.2:c.86+211C=	NP_001339231.1:n.86+211C=
NM_001352303.2:c.278+211C=	NP_001339232.1:n.278+211C=