Canonical Allele Identifier: CA410681911

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868159T>C (hg19) ; chr22:g.19880636T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880636T>C , CM000684.2:g.19880636T>C	GRCh38
NC_000022.10:g.19868159T>C , CM000684.1:g.19868159T>C	GRCh37
NC_000022.9:g.18248159T>C	NCBI36
NG_011835.1:g.66201A>G , LRG_417:g.66201A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1168A>G MANE Select	ENSP00000383365.1:p.Met390Val
ENST00000400518.5:c.1078A>G	ENSP00000383362.1:p.Met360Val
ENST00000400519.6:c.1165A>G	ENSP00000383363.1:p.Met389Val
ENST00000400521.6:c.1168A>G	ENSP00000383365.1:p.Met390Val
ENST00000400525.6:c.1099A>G	ENSP00000383369.3:p.Met367Val
ENST00000462330.5:c.91A>G	ENSP00000485603.2:p.Met31Val
ENST00000462843.2:c.118A>G	ENSP00000485466.2:p.Met40Val
ENST00000474308.5:c.1111A>G	ENSP00000485665.1:p.Met371Val
ENST00000485358.5:c.136A>G	ENSP00000485499.2:p.Met46Val
ENST00000487165.5:n.1262A>G
ENST00000494454.5:n.1242A>G
ENST00000495655.2:n.712A>G
ENST00000542719.6:c.880A>G	ENSP00000485128.2:p.Met294Val
ENST00000634471.1:n.244-365A>G
ENST00000634537.1:c.397A>G	ENSP00000489208.1:p.Met133Val
NM_006440.4:c.1168A>G	NP_006431.2:p.Met390Val
NM_001352300.1:c.1165A>G	NP_001339229.1:p.Met389Val
NM_001352301.1:c.1078A>G	NP_001339230.1:p.Met360Val
NM_001352302.1:c.880A>G	NP_001339231.1:p.Met294Val
NR_147957.1:n.1300A>G
NM_006440.5:c.1168A>G MANE Select	NP_006431.2:p.Met390Val
NM_001352300.2:c.1165A>G	NP_001339229.1:p.Met389Val
NR_147957.2:n.1126A>G
NM_001352301.2:c.1078A>G	NP_001339230.1:p.Met360Val
NM_001352302.2:c.880A>G	NP_001339231.1:p.Met294Val