Canonical Allele Identifier: CA410686436

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882965T>C (hg19) ; chr22:g.19895442T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895442T>C , CM000684.2:g.19895442T>C	GRCh38
NC_000022.10:g.19882965T>C , CM000684.1:g.19882965T>C	GRCh37
NC_000022.9:g.18262965T>C	NCBI36
NG_011835.1:g.51395A>G , LRG_417:g.51395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.914A>G MANE Select	ENSP00000383365.1:p.Asp305Gly
ENST00000334363.14:c.914A>G	ENSP00000334451.9:p.Asp305Gly
ENST00000400518.5:c.824A>G	ENSP00000383362.1:p.Asp275Gly
ENST00000400519.6:c.911A>G	ENSP00000383363.1:p.Asp304Gly
ENST00000400521.6:c.914A>G	ENSP00000383365.1:p.Asp305Gly
ENST00000400525.6:c.845A>G	ENSP00000383369.3:p.Asp282Gly
ENST00000474308.5:c.857A>G	ENSP00000485665.1:p.Asp286Gly
ENST00000475995.3:c.411A>G
ENST00000491939.6:c.818A>G	ENSP00000485543.1:p.Asp273Gly
ENST00000494454.5:n.988A>G
ENST00000542719.6:c.626A>G	ENSP00000485128.2:p.Asp209Gly
ENST00000634537.1:c.143A>G	ENSP00000489208.1:p.Asp48Gly
ENST00000635155.1:n.500A>G
NM_001282512.1:c.914A>G	NP_001269441.1:p.Asp305Gly
NM_006440.4:c.914A>G	NP_006431.2:p.Asp305Gly
NM_001282512.2:c.914A>G	NP_001269441.1:p.Asp305Gly
NM_001352300.1:c.911A>G	NP_001339229.1:p.Asp304Gly
NM_001352301.1:c.824A>G	NP_001339230.1:p.Asp275Gly
NM_001352302.1:c.626A>G	NP_001339231.1:p.Asp209Gly
NM_001352303.1:c.818A>G	NP_001339232.1:p.Asp273Gly
NR_147957.1:n.1046A>G
NM_006440.5:c.914A>G MANE Select	NP_006431.2:p.Asp305Gly
NM_001282512.3:c.914A>G	NP_001269441.1:p.Asp305Gly
NM_001352300.2:c.911A>G	NP_001339229.1:p.Asp304Gly
NR_147957.2:n.872A>G
NM_001352301.2:c.824A>G	NP_001339230.1:p.Asp275Gly
NM_001352302.2:c.626A>G	NP_001339231.1:p.Asp209Gly
NM_001352303.2:c.818A>G	NP_001339232.1:p.Asp273Gly