Canonical Allele Identifier: CA410681921

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868164T>C (hg19) ; chr22:g.19880641T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880641T>C , CM000684.2:g.19880641T>C	GRCh38
NC_000022.10:g.19868164T>C , CM000684.1:g.19868164T>C	GRCh37
NC_000022.9:g.18248164T>C	NCBI36
NG_011835.1:g.66196A>G , LRG_417:g.66196A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1163A>G MANE Select	ENSP00000383365.1:p.Asp388Gly
ENST00000400518.5:c.1073A>G	ENSP00000383362.1:p.Asp358Gly
ENST00000400519.6:c.1160A>G	ENSP00000383363.1:p.Asp387Gly
ENST00000400521.6:c.1163A>G	ENSP00000383365.1:p.Asp388Gly
ENST00000400525.6:c.1094A>G	ENSP00000383369.3:p.Asp365Gly
ENST00000462330.5:c.86A>G	ENSP00000485603.2:p.Asp29Gly
ENST00000462843.2:c.113A>G	ENSP00000485466.2:p.Asp38Gly
ENST00000474308.5:c.1106A>G	ENSP00000485665.1:p.Asp369Gly
ENST00000485358.5:c.131A>G	ENSP00000485499.2:p.Asp44Gly
ENST00000487165.5:n.1257A>G
ENST00000494454.5:n.1237A>G
ENST00000495655.2:n.707A>G
ENST00000542719.6:c.875A>G	ENSP00000485128.2:p.Asp292Gly
ENST00000634471.1:n.244-370A>G
ENST00000634537.1:c.392A>G	ENSP00000489208.1:p.Asp131Gly
NM_006440.4:c.1163A>G	NP_006431.2:p.Asp388Gly
NM_001352300.1:c.1160A>G	NP_001339229.1:p.Asp387Gly
NM_001352301.1:c.1073A>G	NP_001339230.1:p.Asp358Gly
NM_001352302.1:c.875A>G	NP_001339231.1:p.Asp292Gly
NR_147957.1:n.1295A>G
NM_006440.5:c.1163A>G MANE Select	NP_006431.2:p.Asp388Gly
NM_001352300.2:c.1160A>G	NP_001339229.1:p.Asp387Gly
NR_147957.2:n.1121A>G
NM_001352301.2:c.1073A>G	NP_001339230.1:p.Asp358Gly
NM_001352302.2:c.875A>G	NP_001339231.1:p.Asp292Gly