Canonical Allele Identifier: CA2396084492

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19879968C= , CM000684.2:g.19879968C=	GRCh38
NC_000022.10:g.19867491C= , CM000684.1:g.19867491C=	GRCh37
NC_000022.9:g.18247491C=	NCBI36
NG_011835.1:g.66869G= , LRG_417:g.66869G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1275+211G= MANE Select	ENSP00000383365.1:n.1275+211G=
ENST00000400518.5:c.1185+211G=	ENSP00000383362.1:n.1185+211G=
ENST00000400519.6:c.1272+211G=	ENSP00000383363.1:n.1272+211G=
ENST00000400521.6:c.1275+211G=	ENSP00000383365.1:n.1275+211G=
ENST00000400525.6:c.1206+211G=	ENSP00000383369.3:n.1206+211G=
ENST00000462330.5:c.198+211G=	ENSP00000485603.2:n.198+211G=
ENST00000462843.2:c.225+211G=	ENSP00000485466.2:n.225+211G=
ENST00000474308.5:c.1218+211G=	ENSP00000485665.1:n.1218+211G=
ENST00000485358.5:c.243+211G=	ENSP00000485499.2:n.243+211G=
ENST00000487165.5:n.1369+211G=
ENST00000494454.5:n.1349+211G=
ENST00000495655.2:n.819+211G=
ENST00000542719.6:c.987+211G=	ENSP00000485128.2:n.987+211G=
ENST00000634471.1:n.336+211G=
ENST00000634537.1:c.504+211G=	ENSP00000489208.1:n.504+211G=
NM_006440.4:c.1275+211G=	NP_006431.2:n.1275+211G=
NM_001352300.1:c.1272+211G=	NP_001339229.1:n.1272+211G=
NM_001352301.1:c.1185+211G=	NP_001339230.1:n.1185+211G=
NM_001352302.1:c.987+211G=	NP_001339231.1:n.987+211G=
NR_147957.1:n.1407+211G=
NM_006440.5:c.1275+211G= MANE Select	NP_006431.2:n.1275+211G=
NM_001352300.2:c.1272+211G=	NP_001339229.1:n.1272+211G=
NR_147957.2:n.1233+211G=
NM_001352301.2:c.1185+211G=	NP_001339230.1:n.1185+211G=
NM_001352302.2:c.987+211G=	NP_001339231.1:n.987+211G=