Canonical Allele Identifier: CA410682076

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880714-G-C
• MyVariant Identifiers: chr22:g.19868237G>C (hg19) ; chr22:g.19880714G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880714G>C , CM000684.2:g.19880714G>C	GRCh38
NC_000022.10:g.19868237G>C , CM000684.1:g.19868237G>C	GRCh37
NC_000022.9:g.18248237G>C	NCBI36
NG_011835.1:g.66123C>G , LRG_417:g.66123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1090C>G MANE Select	ENSP00000383365.1:p.Arg364Gly
ENST00000400518.5:c.1000C>G	ENSP00000383362.1:p.Arg334Gly
ENST00000400519.6:c.1087C>G	ENSP00000383363.1:p.Arg363Gly
ENST00000400521.6:c.1090C>G	ENSP00000383365.1:p.Arg364Gly
ENST00000400525.6:c.1021C>G	ENSP00000383369.3:p.Arg341Gly
ENST00000462330.5:c.13C>G	ENSP00000485603.2:p.Arg5Gly
ENST00000462843.2:c.40C>G	ENSP00000485466.2:p.Arg14Gly
ENST00000474308.5:c.1033C>G	ENSP00000485665.1:p.Arg345Gly
ENST00000485358.5:c.58C>G	ENSP00000485499.2:p.Arg20Gly
ENST00000487165.5:n.1184C>G
ENST00000494454.5:n.1164C>G
ENST00000495655.2:n.634C>G
ENST00000542719.6:c.802C>G	ENSP00000485128.2:p.Arg268Gly
ENST00000634471.1:n.244-443C>G
ENST00000634537.1:c.319C>G	ENSP00000489208.1:p.Arg107Gly
NM_006440.4:c.1090C>G	NP_006431.2:p.Arg364Gly
NM_001352300.1:c.1087C>G	NP_001339229.1:p.Arg363Gly
NM_001352301.1:c.1000C>G	NP_001339230.1:p.Arg334Gly
NM_001352302.1:c.802C>G	NP_001339231.1:p.Arg268Gly
NR_147957.1:n.1222C>G
NM_006440.5:c.1090C>G MANE Select	NP_006431.2:p.Arg364Gly
NM_001352300.2:c.1087C>G	NP_001339229.1:p.Arg363Gly
NR_147957.2:n.1048C>G
NM_001352301.2:c.1000C>G	NP_001339230.1:p.Arg334Gly
NM_001352302.2:c.802C>G	NP_001339231.1:p.Arg268Gly