Canonical Allele Identifier: CA410682002

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868209A>C (hg19) ; chr22:g.19880686A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880686A>C , CM000684.2:g.19880686A>C	GRCh38
NC_000022.10:g.19868209A>C , CM000684.1:g.19868209A>C	GRCh37
NC_000022.9:g.18248209A>C	NCBI36
NG_011835.1:g.66151T>G , LRG_417:g.66151T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1118T>G MANE Select	ENSP00000383365.1:p.Met373Arg
ENST00000400518.5:c.1028T>G	ENSP00000383362.1:p.Met343Arg
ENST00000400519.6:c.1115T>G	ENSP00000383363.1:p.Met372Arg
ENST00000400521.6:c.1118T>G	ENSP00000383365.1:p.Met373Arg
ENST00000400525.6:c.1049T>G	ENSP00000383369.3:p.Met350Arg
ENST00000462330.5:c.41T>G	ENSP00000485603.2:p.Met14Arg
ENST00000462843.2:c.68T>G	ENSP00000485466.2:p.Met23Arg
ENST00000474308.5:c.1061T>G	ENSP00000485665.1:p.Met354Arg
ENST00000485358.5:c.86T>G	ENSP00000485499.2:p.Met29Arg
ENST00000487165.5:n.1212T>G
ENST00000494454.5:n.1192T>G
ENST00000495655.2:n.662T>G
ENST00000542719.6:c.830T>G	ENSP00000485128.2:p.Met277Arg
ENST00000634471.1:n.244-415T>G
ENST00000634537.1:c.347T>G	ENSP00000489208.1:p.Met116Arg
NM_006440.4:c.1118T>G	NP_006431.2:p.Met373Arg
NM_001352300.1:c.1115T>G	NP_001339229.1:p.Met372Arg
NM_001352301.1:c.1028T>G	NP_001339230.1:p.Met343Arg
NM_001352302.1:c.830T>G	NP_001339231.1:p.Met277Arg
NR_147957.1:n.1250T>G
NM_006440.5:c.1118T>G MANE Select	NP_006431.2:p.Met373Arg
NM_001352300.2:c.1115T>G	NP_001339229.1:p.Met372Arg
NR_147957.2:n.1076T>G
NM_001352301.2:c.1028T>G	NP_001339230.1:p.Met343Arg
NM_001352302.2:c.830T>G	NP_001339231.1:p.Met277Arg