Canonical Allele Identifier: CA1094006611
Gene: TRDN HGNC NCBI

Linked Data

dbSNP Id: rs1775031233

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218744_123218745insACTGATG , CM000668.2:g.123218744_123218745insACTGATG GRCh38
NC_000006.11:g.123539889_123539890insACTGATG , CM000668.1:g.123539889_123539890insACTGATG GRCh37
NC_000006.10:g.123581588_123581589insACTGATG NCBI36
NG_030438.1:g.423349_423350insCATCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2051-5_2051-4insCATCAGT MANE Select ENSP00000333984.5:n.2051-5_2051-4insCATCAGT
ENST00000334268.8:c.2051-5_2051-4insCATCAGT ENSP00000333984.5:n.2051-5_2051-4insCATCAGT
NM_006073.3:c.2051-5_2051-4insCATCAGT NP_006064.2:n.2051-5_2051-4insCATCAGT
XM_011535382.1:c.1970-5_1970-4insCATCAGT XP_011533684.1:n.1970-5_1970-4insCATCAGT
NM_006073.4:c.2051-5_2051-4insCATCAGT MANE Select NP_006064.2:n.2051-5_2051-4insCATCAGT