Canonical Allele Identifier: CA657687312

Gene: TXNRD2

Linked Data

• COSMIC: COSN2495163

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19892053C>T , CM000684.2:g.19892053C>T	GRCh38
NC_000022.10:g.19879576C>T , CM000684.1:g.19879576C>T	GRCh37
NC_000022.9:g.18259576C>T	NCBI36
NG_011835.1:g.54784G>A , LRG_417:g.54784G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.949+3354G>A MANE Select	ENSP00000383365.1:n.949+3354G>A
ENST00000400518.5:c.859+3354G>A	ENSP00000383362.1:n.859+3354G>A
ENST00000400519.6:c.946+3354G>A	ENSP00000383363.1:n.946+3354G>A
ENST00000400521.6:c.949+3354G>A	ENSP00000383365.1:n.949+3354G>A
ENST00000400525.6:c.880+3354G>A	ENSP00000383369.3:n.880+3354G>A
ENST00000474308.5:c.892+3354G>A	ENSP00000485665.1:n.892+3354G>A
ENST00000494454.5:n.1023+3354G>A
ENST00000542719.6:c.661+3354G>A	ENSP00000485128.2:n.661+3354G>A
ENST00000634537.1:c.178+3354G>A	ENSP00000489208.1:n.178+3354G>A
ENST00000635155.1:n.536-293G>A
NM_006440.4:c.949+3354G>A	NP_006431.2:n.949+3354G>A
NM_001352300.1:c.946+3354G>A	NP_001339229.1:n.946+3354G>A
NM_001352301.1:c.859+3354G>A	NP_001339230.1:n.859+3354G>A
NM_001352302.1:c.661+3354G>A	NP_001339231.1:n.661+3354G>A
NR_147957.1:n.1081+3354G>A
NM_006440.5:c.949+3354G>A MANE Select	NP_006431.2:n.949+3354G>A
NM_001352300.2:c.946+3354G>A	NP_001339229.1:n.946+3354G>A
NR_147957.2:n.907+3354G>A
NM_001352301.2:c.859+3354G>A	NP_001339230.1:n.859+3354G>A
NM_001352302.2:c.661+3354G>A	NP_001339231.1:n.661+3354G>A