Canonical Allele Identifier: CA2396084885
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1938735336

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19880718del , CM000684.2:g.19880718del GRCh38
NC_000022.10:g.19868241del , CM000684.1:g.19868241del GRCh37
NC_000022.9:g.18248241del NCBI36
NG_011835.1:g.66122del , LRG_417:g.66122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.1089del
ENST00000400518.5:c.999del
ENST00000400519.6:c.1086del
ENST00000400521.6:c.1089del
ENST00000400525.6:c.1020del
ENST00000462330.5:c.12del
ENST00000462843.2:c.39del
ENST00000474308.5:c.1032del
ENST00000485358.5:c.57del
ENST00000487165.5:n.1183del
ENST00000494454.5:n.1163del
ENST00000495655.2:n.633del
ENST00000542719.6:c.801del
ENST00000634471.1:n.244-444del
ENST00000634537.1:c.318del
NM_006440.4:c.1089del
NM_001352300.1:c.1086del
NM_001352301.1:c.999del
NM_001352302.1:c.801del
NR_147957.1:n.1221del
NM_006440.5:c.1089del
NM_001352300.2:c.1086del
NR_147957.2:n.1047del
NM_001352301.2:c.999del
NM_001352302.2:c.801del