Canonical Allele Identifier: CA410681913

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868161A>C (hg19) ; chr22:g.19880638A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880638A>C , CM000684.2:g.19880638A>C	GRCh38
NC_000022.10:g.19868161A>C , CM000684.1:g.19868161A>C	GRCh37
NC_000022.9:g.18248161A>C	NCBI36
NG_011835.1:g.66199T>G , LRG_417:g.66199T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1166T>G MANE Select	ENSP00000383365.1:p.Leu389Arg
ENST00000400518.5:c.1076T>G	ENSP00000383362.1:p.Leu359Arg
ENST00000400519.6:c.1163T>G	ENSP00000383363.1:p.Leu388Arg
ENST00000400521.6:c.1166T>G	ENSP00000383365.1:p.Leu389Arg
ENST00000400525.6:c.1097T>G	ENSP00000383369.3:p.Leu366Arg
ENST00000462330.5:c.89T>G	ENSP00000485603.2:p.Leu30Arg
ENST00000462843.2:c.116T>G	ENSP00000485466.2:p.Leu39Arg
ENST00000474308.5:c.1109T>G	ENSP00000485665.1:p.Leu370Arg
ENST00000485358.5:c.134T>G	ENSP00000485499.2:p.Leu45Arg
ENST00000487165.5:n.1260T>G
ENST00000494454.5:n.1240T>G
ENST00000495655.2:n.710T>G
ENST00000542719.6:c.878T>G	ENSP00000485128.2:p.Leu293Arg
ENST00000634471.1:n.244-367T>G
ENST00000634537.1:c.395T>G	ENSP00000489208.1:p.Leu132Arg
NM_006440.4:c.1166T>G	NP_006431.2:p.Leu389Arg
NM_001352300.1:c.1163T>G	NP_001339229.1:p.Leu388Arg
NM_001352301.1:c.1076T>G	NP_001339230.1:p.Leu359Arg
NM_001352302.1:c.878T>G	NP_001339231.1:p.Leu293Arg
NR_147957.1:n.1298T>G
NM_006440.5:c.1166T>G MANE Select	NP_006431.2:p.Leu389Arg
NM_001352300.2:c.1163T>G	NP_001339229.1:p.Leu388Arg
NR_147957.2:n.1124T>G
NM_001352301.2:c.1076T>G	NP_001339230.1:p.Leu359Arg
NM_001352302.2:c.878T>G	NP_001339231.1:p.Leu293Arg