Canonical Allele Identifier: CA410681923

Gene: TXNRD2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1162G>T MANE Select	ENSP00000383365.1:p.Asp388Tyr
ENST00000400518.5:c.1072G>T	ENSP00000383362.1:p.Asp358Tyr
ENST00000400519.6:c.1159G>T	ENSP00000383363.1:p.Asp387Tyr
ENST00000400521.6:c.1162G>T	ENSP00000383365.1:p.Asp388Tyr
ENST00000400525.6:c.1093G>T	ENSP00000383369.3:p.Asp365Tyr
ENST00000462330.5:c.85G>T	ENSP00000485603.2:p.Asp29Tyr
ENST00000462843.2:c.112G>T	ENSP00000485466.2:p.Asp38Tyr
ENST00000474308.5:c.1105G>T	ENSP00000485665.1:p.Asp369Tyr
ENST00000485358.5:c.130G>T	ENSP00000485499.2:p.Asp44Tyr
ENST00000487165.5:n.1256G>T
ENST00000494454.5:n.1236G>T
ENST00000495655.2:n.706G>T
ENST00000542719.6:c.874G>T	ENSP00000485128.2:p.Asp292Tyr
ENST00000634471.1:n.244-371G>T
ENST00000634537.1:c.391G>T	ENSP00000489208.1:p.Asp131Tyr
NM_006440.4:c.1162G>T	NP_006431.2:p.Asp388Tyr
NM_001352300.1:c.1159G>T	NP_001339229.1:p.Asp387Tyr
NM_001352301.1:c.1072G>T	NP_001339230.1:p.Asp358Tyr
NM_001352302.1:c.874G>T	NP_001339231.1:p.Asp292Tyr
NR_147957.1:n.1294G>T
NM_006440.5:c.1162G>T MANE Select	NP_006431.2:p.Asp388Tyr
NM_001352300.2:c.1159G>T	NP_001339229.1:p.Asp387Tyr
NR_147957.2:n.1120G>T
NM_001352301.2:c.1072G>T	NP_001339230.1:p.Asp358Tyr
NM_001352302.2:c.874G>T	NP_001339231.1:p.Asp292Tyr