Canonical Allele Identifier: CA410681964

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868188T>G (hg19) ; chr22:g.19880665T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880665T>G , CM000684.2:g.19880665T>G	GRCh38
NC_000022.10:g.19868188T>G , CM000684.1:g.19868188T>G	GRCh37
NC_000022.9:g.18248188T>G	NCBI36
NG_011835.1:g.66172A>C , LRG_417:g.66172A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1139A>C MANE Select	ENSP00000383365.1:p.Gln380Pro
ENST00000400518.5:c.1049A>C	ENSP00000383362.1:p.Gln350Pro
ENST00000400519.6:c.1136A>C	ENSP00000383363.1:p.Gln379Pro
ENST00000400521.6:c.1139A>C	ENSP00000383365.1:p.Gln380Pro
ENST00000400525.6:c.1070A>C	ENSP00000383369.3:p.Gln357Pro
ENST00000462330.5:c.62A>C	ENSP00000485603.2:p.Gln21Pro
ENST00000462843.2:c.89A>C	ENSP00000485466.2:p.Gln30Pro
ENST00000474308.5:c.1082A>C	ENSP00000485665.1:p.Gln361Pro
ENST00000485358.5:c.107A>C	ENSP00000485499.2:p.Gln36Pro
ENST00000487165.5:n.1233A>C
ENST00000494454.5:n.1213A>C
ENST00000495655.2:n.683A>C
ENST00000542719.6:c.851A>C	ENSP00000485128.2:p.Gln284Pro
ENST00000634471.1:n.244-394A>C
ENST00000634537.1:c.368A>C	ENSP00000489208.1:p.Gln123Pro
NM_006440.4:c.1139A>C	NP_006431.2:p.Gln380Pro
NM_001352300.1:c.1136A>C	NP_001339229.1:p.Gln379Pro
NM_001352301.1:c.1049A>C	NP_001339230.1:p.Gln350Pro
NM_001352302.1:c.851A>C	NP_001339231.1:p.Gln284Pro
NR_147957.1:n.1271A>C
NM_006440.5:c.1139A>C MANE Select	NP_006431.2:p.Gln380Pro
NM_001352300.2:c.1136A>C	NP_001339229.1:p.Gln379Pro
NR_147957.2:n.1097A>C
NM_001352301.2:c.1049A>C	NP_001339230.1:p.Gln350Pro
NM_001352302.2:c.851A>C	NP_001339231.1:p.Gln284Pro