Canonical Allele Identifier: CA2655323862

Gene: TXNRD2

Linked Data

• ClinVar Variation Id: 2800078
• ClinVar RCV Id: RCV003620558
• gnomAD v4: 22-19880730-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880731dup , CM000684.2:g.19880731dup	GRCh38
NC_000022.10:g.19868254dup , CM000684.1:g.19868254dup	GRCh37
NC_000022.9:g.18248254dup	NCBI36
NG_011835.1:g.66106dup , LRG_417:g.66106dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1087-14dup MANE Select	ENSP00000383365.1:n.1087-14dup
ENST00000400518.5:c.997-14dup	ENSP00000383362.1:n.997-14dup
ENST00000400519.6:c.1084-14dup	ENSP00000383363.1:n.1084-14dup
ENST00000400521.6:c.1087-14dup	ENSP00000383365.1:n.1087-14dup
ENST00000400525.6:c.1018-14dup	ENSP00000383369.3:n.1018-14dup
ENST00000462330.5:c.10-14dup	ENSP00000485603.2:n.10-14dup
ENST00000462843.2:c.37-14dup	ENSP00000485466.2:n.37-14dup
ENST00000474308.5:c.1030-14dup	ENSP00000485665.1:n.1030-14dup
ENST00000485358.5:c.55-14dup	ENSP00000485499.2:n.55-14dup
ENST00000487165.5:n.1181-14dup
ENST00000494454.5:n.1161-14dup
ENST00000495655.2:n.617dup
ENST00000542719.6:c.799-14dup	ENSP00000485128.2:n.799-14dup
ENST00000634471.1:n.244-460dup
ENST00000634537.1:c.316-14dup	ENSP00000489208.1:n.316-14dup
NM_006440.4:c.1087-14dup	NP_006431.2:n.1087-14dup
NM_001352300.1:c.1084-14dup	NP_001339229.1:n.1084-14dup
NM_001352301.1:c.997-14dup	NP_001339230.1:n.997-14dup
NM_001352302.1:c.799-14dup	NP_001339231.1:n.799-14dup
NR_147957.1:n.1219-14dup
NM_006440.5:c.1087-14dup MANE Select	NP_006431.2:n.1087-14dup
NM_001352300.2:c.1084-14dup	NP_001339229.1:n.1084-14dup
NR_147957.2:n.1045-14dup
NM_001352301.2:c.997-14dup	NP_001339230.1:n.997-14dup
NM_001352302.2:c.799-14dup	NP_001339231.1:n.799-14dup