Canonical Allele Identifier: CA410686686

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883054G>T (hg19) ; chr22:g.19895531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895531G>T , CM000684.2:g.19895531G>T	GRCh38
NC_000022.10:g.19883054G>T , CM000684.1:g.19883054G>T	GRCh37
NC_000022.9:g.18263054G>T	NCBI36
NG_011835.1:g.51306C>A , LRG_417:g.51306C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.825C>A MANE Select	ENSP00000383365.1:p.Phe275Leu
ENST00000334363.14:c.825C>A	ENSP00000334451.9:p.Phe275Leu
ENST00000400518.5:c.735C>A	ENSP00000383362.1:p.Phe245Leu
ENST00000400519.6:c.822C>A	ENSP00000383363.1:p.Phe274Leu
ENST00000400521.6:c.825C>A	ENSP00000383365.1:p.Phe275Leu
ENST00000400525.6:c.756C>A	ENSP00000383369.3:p.Phe252Leu
ENST00000474308.5:c.768C>A	ENSP00000485665.1:p.Phe256Leu
ENST00000475995.3:c.322C>A
ENST00000491939.6:c.729C>A	ENSP00000485543.1:p.Phe243Leu
ENST00000494454.5:n.899C>A
ENST00000542719.6:c.537C>A	ENSP00000485128.2:p.Phe179Leu
ENST00000634537.1:c.54C>A	ENSP00000489208.1:p.Phe18Leu
ENST00000635155.1:n.411C>A
NM_001282512.1:c.825C>A	NP_001269441.1:p.Phe275Leu
NM_006440.4:c.825C>A	NP_006431.2:p.Phe275Leu
NM_001282512.2:c.825C>A	NP_001269441.1:p.Phe275Leu
NM_001352300.1:c.822C>A	NP_001339229.1:p.Phe274Leu
NM_001352301.1:c.735C>A	NP_001339230.1:p.Phe245Leu
NM_001352302.1:c.537C>A	NP_001339231.1:p.Phe179Leu
NM_001352303.1:c.729C>A	NP_001339232.1:p.Phe243Leu
NR_147957.1:n.957C>A
NM_006440.5:c.825C>A MANE Select	NP_006431.2:p.Phe275Leu
NM_001282512.3:c.825C>A	NP_001269441.1:p.Phe275Leu
NM_001352300.2:c.822C>A	NP_001339229.1:p.Phe274Leu
NR_147957.2:n.783C>A
NM_001352301.2:c.735C>A	NP_001339230.1:p.Phe245Leu
NM_001352302.2:c.537C>A	NP_001339231.1:p.Phe179Leu
NM_001352303.2:c.729C>A	NP_001339232.1:p.Phe243Leu