Canonical Allele Identifier: CA410681912
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.1168A>C MANE Select ENSP00000383365.1:p.Met390Leu
ENST00000400518.5:c.1078A>C ENSP00000383362.1:p.Met360Leu
ENST00000400519.6:c.1165A>C ENSP00000383363.1:p.Met389Leu
ENST00000400521.6:c.1168A>C ENSP00000383365.1:p.Met390Leu
ENST00000400525.6:c.1099A>C ENSP00000383369.3:p.Met367Leu
ENST00000462330.5:c.91A>C ENSP00000485603.2:p.Met31Leu
ENST00000462843.2:c.118A>C ENSP00000485466.2:p.Met40Leu
ENST00000474308.5:c.1111A>C ENSP00000485665.1:p.Met371Leu
ENST00000485358.5:c.136A>C ENSP00000485499.2:p.Met46Leu
ENST00000487165.5:n.1262A>C
ENST00000494454.5:n.1242A>C
ENST00000495655.2:n.712A>C
ENST00000542719.6:c.880A>C ENSP00000485128.2:p.Met294Leu
ENST00000634471.1:n.244-365A>C
ENST00000634537.1:c.397A>C ENSP00000489208.1:p.Met133Leu
NM_006440.4:c.1168A>C NP_006431.2:p.Met390Leu
NM_001352300.1:c.1165A>C NP_001339229.1:p.Met389Leu
NM_001352301.1:c.1078A>C NP_001339230.1:p.Met360Leu
NM_001352302.1:c.880A>C NP_001339231.1:p.Met294Leu
NR_147957.1:n.1300A>C
NM_006440.5:c.1168A>C MANE Select NP_006431.2:p.Met390Leu
NM_001352300.2:c.1165A>C NP_001339229.1:p.Met389Leu
NR_147957.2:n.1126A>C
NM_001352301.2:c.1078A>C NP_001339230.1:p.Met360Leu
NM_001352302.2:c.880A>C NP_001339231.1:p.Met294Leu