Canonical Allele Identifier: CA10103714

Gene: TXNRD2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19878452C>T , CM000684.2:g.19878452C>T	GRCh38
NC_000022.10:g.19865975C>T , CM000684.1:g.19865975C>T	GRCh37
NC_000022.9:g.18245975C>T	NCBI36
NG_011835.1:g.68385G>A , LRG_417:g.68385G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1276-15G>A MANE Select	ENSP00000383365.1:n.1276-15G>A
ENST00000400518.5:c.1186-15G>A	ENSP00000383362.1:n.1186-15G>A
ENST00000400519.6:c.1273-15G>A	ENSP00000383363.1:n.1273-15G>A
ENST00000400521.6:c.1276-15G>A	ENSP00000383365.1:n.1276-15G>A
ENST00000400525.6:c.1207-15G>A	ENSP00000383369.3:n.1207-15G>A
ENST00000462330.5:c.199-15G>A	ENSP00000485603.2:n.199-15G>A
ENST00000462843.2:c.226-15G>A	ENSP00000485466.2:n.226-15G>A
ENST00000474308.5:c.1219-15G>A	ENSP00000485665.1:n.1219-15G>A
ENST00000485358.5:c.244-15G>A	ENSP00000485499.2:n.244-15G>A
ENST00000487165.5:n.1370-15G>A
ENST00000494454.5:n.1350-15G>A
ENST00000495655.2:n.820-15G>A
ENST00000542719.6:c.988-15G>A	ENSP00000485128.2:n.988-15G>A
ENST00000634471.1:n.337-15G>A
ENST00000634537.1:c.505-15G>A	ENSP00000489208.1:n.505-15G>A
NM_006440.4:c.1276-15G>A	NP_006431.2:n.1276-15G>A
NM_001352300.1:c.1273-15G>A	NP_001339229.1:n.1273-15G>A
NM_001352301.1:c.1186-15G>A	NP_001339230.1:n.1186-15G>A
NM_001352302.1:c.988-15G>A	NP_001339231.1:n.988-15G>A
NR_147957.1:n.1408-15G>A
NM_006440.5:c.1276-15G>A MANE Select	NP_006431.2:n.1276-15G>A
NM_001352300.2:c.1273-15G>A	NP_001339229.1:n.1273-15G>A
NR_147957.2:n.1234-15G>A
NM_001352301.2:c.1186-15G>A	NP_001339230.1:n.1186-15G>A
NM_001352302.2:c.988-15G>A	NP_001339231.1:n.988-15G>A