Canonical Allele Identifier: CA410681924

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868165C>T (hg19) ; chr22:g.19880642C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880642C>T , CM000684.2:g.19880642C>T	GRCh38
NC_000022.10:g.19868165C>T , CM000684.1:g.19868165C>T	GRCh37
NC_000022.9:g.18248165C>T	NCBI36
NG_011835.1:g.66195G>A , LRG_417:g.66195G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1162G>A MANE Select	ENSP00000383365.1:p.Asp388Asn
ENST00000400518.5:c.1072G>A	ENSP00000383362.1:p.Asp358Asn
ENST00000400519.6:c.1159G>A	ENSP00000383363.1:p.Asp387Asn
ENST00000400521.6:c.1162G>A	ENSP00000383365.1:p.Asp388Asn
ENST00000400525.6:c.1093G>A	ENSP00000383369.3:p.Asp365Asn
ENST00000462330.5:c.85G>A	ENSP00000485603.2:p.Asp29Asn
ENST00000462843.2:c.112G>A	ENSP00000485466.2:p.Asp38Asn
ENST00000474308.5:c.1105G>A	ENSP00000485665.1:p.Asp369Asn
ENST00000485358.5:c.130G>A	ENSP00000485499.2:p.Asp44Asn
ENST00000487165.5:n.1256G>A
ENST00000494454.5:n.1236G>A
ENST00000495655.2:n.706G>A
ENST00000542719.6:c.874G>A	ENSP00000485128.2:p.Asp292Asn
ENST00000634471.1:n.244-371G>A
ENST00000634537.1:c.391G>A	ENSP00000489208.1:p.Asp131Asn
NM_006440.4:c.1162G>A	NP_006431.2:p.Asp388Asn
NM_001352300.1:c.1159G>A	NP_001339229.1:p.Asp387Asn
NM_001352301.1:c.1072G>A	NP_001339230.1:p.Asp358Asn
NM_001352302.1:c.874G>A	NP_001339231.1:p.Asp292Asn
NR_147957.1:n.1294G>A
NM_006440.5:c.1162G>A MANE Select	NP_006431.2:p.Asp388Asn
NM_001352300.2:c.1159G>A	NP_001339229.1:p.Asp387Asn
NR_147957.2:n.1120G>A
NM_001352301.2:c.1072G>A	NP_001339230.1:p.Asp358Asn
NM_001352302.2:c.874G>A	NP_001339231.1:p.Asp292Asn