Canonical Allele Identifier: CA410681922

Gene: TXNRD2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1163A>C MANE Select	ENSP00000383365.1:p.Asp388Ala
ENST00000400518.5:c.1073A>C	ENSP00000383362.1:p.Asp358Ala
ENST00000400519.6:c.1160A>C	ENSP00000383363.1:p.Asp387Ala
ENST00000400521.6:c.1163A>C	ENSP00000383365.1:p.Asp388Ala
ENST00000400525.6:c.1094A>C	ENSP00000383369.3:p.Asp365Ala
ENST00000462330.5:c.86A>C	ENSP00000485603.2:p.Asp29Ala
ENST00000462843.2:c.113A>C	ENSP00000485466.2:p.Asp38Ala
ENST00000474308.5:c.1106A>C	ENSP00000485665.1:p.Asp369Ala
ENST00000485358.5:c.131A>C	ENSP00000485499.2:p.Asp44Ala
ENST00000487165.5:n.1257A>C
ENST00000494454.5:n.1237A>C
ENST00000495655.2:n.707A>C
ENST00000542719.6:c.875A>C	ENSP00000485128.2:p.Asp292Ala
ENST00000634471.1:n.244-370A>C
ENST00000634537.1:c.392A>C	ENSP00000489208.1:p.Asp131Ala
NM_006440.4:c.1163A>C	NP_006431.2:p.Asp388Ala
NM_001352300.1:c.1160A>C	NP_001339229.1:p.Asp387Ala
NM_001352301.1:c.1073A>C	NP_001339230.1:p.Asp358Ala
NM_001352302.1:c.875A>C	NP_001339231.1:p.Asp292Ala
NR_147957.1:n.1295A>C
NM_006440.5:c.1163A>C MANE Select	NP_006431.2:p.Asp388Ala
NM_001352300.2:c.1160A>C	NP_001339229.1:p.Asp387Ala
NR_147957.2:n.1121A>C
NM_001352301.2:c.1073A>C	NP_001339230.1:p.Asp358Ala
NM_001352302.2:c.875A>C	NP_001339231.1:p.Asp292Ala