Canonical Allele Identifier: CA410686665

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883044A>C (hg19) ; chr22:g.19895521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895521A>C , CM000684.2:g.19895521A>C	GRCh38
NC_000022.10:g.19883044A>C , CM000684.1:g.19883044A>C	GRCh37
NC_000022.9:g.18263044A>C	NCBI36
NG_011835.1:g.51316T>G , LRG_417:g.51316T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.835T>G MANE Select	ENSP00000383365.1:p.Cys279Gly
ENST00000334363.14:c.835T>G	ENSP00000334451.9:p.Cys279Gly
ENST00000400518.5:c.745T>G	ENSP00000383362.1:p.Cys249Gly
ENST00000400519.6:c.832T>G	ENSP00000383363.1:p.Cys278Gly
ENST00000400521.6:c.835T>G	ENSP00000383365.1:p.Cys279Gly
ENST00000400525.6:c.766T>G	ENSP00000383369.3:p.Cys256Gly
ENST00000474308.5:c.778T>G	ENSP00000485665.1:p.Cys260Gly
ENST00000475995.3:c.332T>G
ENST00000491939.6:c.739T>G	ENSP00000485543.1:p.Cys247Gly
ENST00000494454.5:n.909T>G
ENST00000542719.6:c.547T>G	ENSP00000485128.2:p.Cys183Gly
ENST00000634537.1:c.64T>G	ENSP00000489208.1:p.Cys22Gly
ENST00000635155.1:n.421T>G
NM_001282512.1:c.835T>G	NP_001269441.1:p.Cys279Gly
NM_006440.4:c.835T>G	NP_006431.2:p.Cys279Gly
NM_001282512.2:c.835T>G	NP_001269441.1:p.Cys279Gly
NM_001352300.1:c.832T>G	NP_001339229.1:p.Cys278Gly
NM_001352301.1:c.745T>G	NP_001339230.1:p.Cys249Gly
NM_001352302.1:c.547T>G	NP_001339231.1:p.Cys183Gly
NM_001352303.1:c.739T>G	NP_001339232.1:p.Cys247Gly
NR_147957.1:n.967T>G
NM_006440.5:c.835T>G MANE Select	NP_006431.2:p.Cys279Gly
NM_001282512.3:c.835T>G	NP_001269441.1:p.Cys279Gly
NM_001352300.2:c.832T>G	NP_001339229.1:p.Cys278Gly
NR_147957.2:n.793T>G
NM_001352301.2:c.745T>G	NP_001339230.1:p.Cys249Gly
NM_001352302.2:c.547T>G	NP_001339231.1:p.Cys183Gly
NM_001352303.2:c.739T>G	NP_001339232.1:p.Cys247Gly