Canonical Allele Identifier: CA13630613

Gene: TXNRD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.104287004C>G , CM000674.2:g.104287004C>G	GRCh38
NC_000012.11:g.104680782C>G , CM000674.1:g.104680782C>G	GRCh37
NC_000012.10:g.103204912C>G	NCBI36
NG_029392.1:g.76224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525566.6:c.305-1927C>G MANE Select	ENSP00000434516.1:n.305-1927C>G
ENST00000354940.10:c.-379C>G	ENSP00000347020.7:n.-379C>G
ENST00000388854.7:c.-424C>G	ENSP00000373506.4:n.-424C>G
ENST00000397736.6:c.-243C>G	ENSP00000380844.3:n.-243C>G
ENST00000429002.6:c.305-1927C>G	ENSP00000412045.4:n.305-1927C>G
ENST00000503506.6:c.-252C>G	ENSP00000421934.2:n.-252C>G
ENST00000525566.5:c.305-1927C>G	ENSP00000434516.1:n.305-1927C>G
ENST00000526266.5:c.-208-44C>G	ENSP00000431294.1:n.-208-44C>G
ENST00000526390.5:c.-309C>G	ENSP00000435123.1:n.-309C>G
ENST00000526691.5:c.-333C>G	ENSP00000435929.1:n.-333C>G
ENST00000531689.5:c.-329C>G	ENSP00000433507.1:n.-329C>G
ENST00000531691.5:c.-232C>G	ENSP00000431925.1:n.-232C>G
NM_001093771.2:c.305-1927C>G	NP_001087240.1:n.305-1927C>G
NM_001261445.1:c.-424C>G	NP_001248374.1:n.-424C>G
NM_001261446.1:c.-243C>G	NP_001248375.1:n.-243C>G
NM_003330.3:c.-333C>G	NP_003321.3:n.-333C>G
NM_182729.2:c.-252C>G	NP_877393.1:n.-252C>G
NM_182742.2:c.-379C>G	NP_877419.1:n.-379C>G
NM_182743.2:c.-142C>G	NP_877420.1:n.-142C>G
NM_001093771.3:c.305-1927C>G MANE Select	NP_001087240.1:n.305-1927C>G