Canonical Allele Identifier: CA2396084468

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19879918A= , CM000684.2:g.19879918A=	GRCh38
NC_000022.10:g.19867441A= , CM000684.1:g.19867441A=	GRCh37
NC_000022.9:g.18247441A=	NCBI36
NG_011835.1:g.66919T= , LRG_417:g.66919T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1275+261T= MANE Select	ENSP00000383365.1:n.1275+261T=
ENST00000400518.5:c.1185+261T=	ENSP00000383362.1:n.1185+261T=
ENST00000400519.6:c.1272+261T=	ENSP00000383363.1:n.1272+261T=
ENST00000400521.6:c.1275+261T=	ENSP00000383365.1:n.1275+261T=
ENST00000400525.6:c.1206+261T=	ENSP00000383369.3:n.1206+261T=
ENST00000462330.5:c.198+261T=	ENSP00000485603.2:n.198+261T=
ENST00000462843.2:c.225+261T=	ENSP00000485466.2:n.225+261T=
ENST00000474308.5:c.1218+261T=	ENSP00000485665.1:n.1218+261T=
ENST00000485358.5:c.243+261T=	ENSP00000485499.2:n.243+261T=
ENST00000487165.5:n.1369+261T=
ENST00000494454.5:n.1349+261T=
ENST00000495655.2:n.819+261T=
ENST00000542719.6:c.987+261T=	ENSP00000485128.2:n.987+261T=
ENST00000634471.1:n.336+261T=
ENST00000634537.1:c.504+261T=	ENSP00000489208.1:n.504+261T=
NM_006440.4:c.1275+261T=	NP_006431.2:n.1275+261T=
NM_001352300.1:c.1272+261T=	NP_001339229.1:n.1272+261T=
NM_001352301.1:c.1185+261T=	NP_001339230.1:n.1185+261T=
NM_001352302.1:c.987+261T=	NP_001339231.1:n.987+261T=
NR_147957.1:n.1407+261T=
NM_006440.5:c.1275+261T= MANE Select	NP_006431.2:n.1275+261T=
NM_001352300.2:c.1272+261T=	NP_001339229.1:n.1272+261T=
NR_147957.2:n.1233+261T=
NM_001352301.2:c.1185+261T=	NP_001339230.1:n.1185+261T=
NM_001352302.2:c.987+261T=	NP_001339231.1:n.987+261T=