Canonical Allele Identifier: CA410681892

Gene: TXNRD2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880628G>C , CM000684.2:g.19880628G>C	GRCh38
NC_000022.10:g.19868151G>C , CM000684.1:g.19868151G>C	GRCh37
NC_000022.9:g.18248151G>C	NCBI36
NG_011835.1:g.66209C>G , LRG_417:g.66209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1176C>G MANE Select	ENSP00000383365.1:p.Tyr392Ter
ENST00000400518.5:c.1086C>G	ENSP00000383362.1:p.Tyr362Ter
ENST00000400519.6:c.1173C>G	ENSP00000383363.1:p.Tyr391Ter
ENST00000400521.6:c.1176C>G	ENSP00000383365.1:p.Tyr392Ter
ENST00000400525.6:c.1107C>G	ENSP00000383369.3:p.Tyr369Ter
ENST00000462330.5:c.99C>G	ENSP00000485603.2:p.Tyr33Ter
ENST00000462843.2:c.126C>G	ENSP00000485466.2:p.Tyr42Ter
ENST00000474308.5:c.1119C>G	ENSP00000485665.1:p.Tyr373Ter
ENST00000485358.5:c.144C>G	ENSP00000485499.2:p.Tyr48Ter
ENST00000487165.5:n.1270C>G
ENST00000494454.5:n.1250C>G
ENST00000495655.2:n.720C>G
ENST00000542719.6:c.888C>G	ENSP00000485128.2:p.Tyr296Ter
ENST00000634471.1:n.244-357C>G
ENST00000634537.1:c.405C>G	ENSP00000489208.1:p.Tyr135Ter
NM_006440.4:c.1176C>G	NP_006431.2:p.Tyr392Ter
NM_001352300.1:c.1173C>G	NP_001339229.1:p.Tyr391Ter
NM_001352301.1:c.1086C>G	NP_001339230.1:p.Tyr362Ter
NM_001352302.1:c.888C>G	NP_001339231.1:p.Tyr296Ter
NR_147957.1:n.1308C>G
NM_006440.5:c.1176C>G MANE Select	NP_006431.2:p.Tyr392Ter
NM_001352300.2:c.1173C>G	NP_001339229.1:p.Tyr391Ter
NR_147957.2:n.1134C>G
NM_001352301.2:c.1086C>G	NP_001339230.1:p.Tyr362Ter
NM_001352302.2:c.888C>G	NP_001339231.1:p.Tyr296Ter