Canonical Allele Identifier: CA410681896

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880630-A-C
• MyVariant Identifiers: chr22:g.19868153A>C (hg19) ; chr22:g.19880630A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880630A>C , CM000684.2:g.19880630A>C	GRCh38
NC_000022.10:g.19868153A>C , CM000684.1:g.19868153A>C	GRCh37
NC_000022.9:g.18248153A>C	NCBI36
NG_011835.1:g.66207T>G , LRG_417:g.66207T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1174T>G MANE Select	ENSP00000383365.1:p.Tyr392Asp
ENST00000400518.5:c.1084T>G	ENSP00000383362.1:p.Tyr362Asp
ENST00000400519.6:c.1171T>G	ENSP00000383363.1:p.Tyr391Asp
ENST00000400521.6:c.1174T>G	ENSP00000383365.1:p.Tyr392Asp
ENST00000400525.6:c.1105T>G	ENSP00000383369.3:p.Tyr369Asp
ENST00000462330.5:c.97T>G	ENSP00000485603.2:p.Tyr33Asp
ENST00000462843.2:c.124T>G	ENSP00000485466.2:p.Tyr42Asp
ENST00000474308.5:c.1117T>G	ENSP00000485665.1:p.Tyr373Asp
ENST00000485358.5:c.142T>G	ENSP00000485499.2:p.Tyr48Asp
ENST00000487165.5:n.1268T>G
ENST00000494454.5:n.1248T>G
ENST00000495655.2:n.718T>G
ENST00000542719.6:c.886T>G	ENSP00000485128.2:p.Tyr296Asp
ENST00000634471.1:n.244-359T>G
ENST00000634537.1:c.403T>G	ENSP00000489208.1:p.Tyr135Asp
NM_006440.4:c.1174T>G	NP_006431.2:p.Tyr392Asp
NM_001352300.1:c.1171T>G	NP_001339229.1:p.Tyr391Asp
NM_001352301.1:c.1084T>G	NP_001339230.1:p.Tyr362Asp
NM_001352302.1:c.886T>G	NP_001339231.1:p.Tyr296Asp
NR_147957.1:n.1306T>G
NM_006440.5:c.1174T>G MANE Select	NP_006431.2:p.Tyr392Asp
NM_001352300.2:c.1171T>G	NP_001339229.1:p.Tyr391Asp
NR_147957.2:n.1132T>G
NM_001352301.2:c.1084T>G	NP_001339230.1:p.Tyr362Asp
NM_001352302.2:c.886T>G	NP_001339231.1:p.Tyr296Asp