Canonical Allele Identifier: CA16611945
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 408737
ClinVar RCV Id: RCV002526417
dbSNP Id: rs1060502114
MyVariant Identifiers: chr6:g.123825039del (hg19) chr6:g.123503894del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123503894del , CM000668.2:g.123503894del GRCh38
NC_000006.11:g.123825039del , CM000668.1:g.123825039del GRCh37
NC_000006.10:g.123866738del NCBI36
NG_030438.1:g.138200del

Transcript Alleles

HGVS Amino-acid change
ENST00000361029.9:c.420del ENSP00000354307.5:p.Ala142LeufsTer15
ENST00000546248.6:c.618del ENSP00000439281.2:p.Ala208LeufsTer15
ENST00000334268.9:c.618del MANE Select ENSP00000333984.5:p.Ala208LeufsTer15
ENST00000662930.1:c.618del ENSP00000499585.1:p.Ala208LeufsTer15
ENST00000334268.8:c.618del ENSP00000333984.5:p.Ala208LeufsTer15
ENST00000361029.8:c.134del
ENST00000546248.5:c.618del ENSP00000439281.2:p.Ala208LeufsTer15
ENST00000628709.2:c.618del ENSP00000486095.1:p.Ala208LeufsTer15
NM_001251987.1:c.618del NP_001238916.1:p.Ala208LeufsTer15
NM_001256020.1:c.618del NP_001242949.1:p.Ala208LeufsTer15
NM_001256021.1:c.618del NP_001242950.1:p.Ala208LeufsTer15
NM_006073.3:c.618del NP_006064.2:p.Ala208LeufsTer15
XM_011535382.1:c.618del XP_011533684.1:p.Ala208LeufsTer15
NM_006073.4:c.618del MANE Select NP_006064.2:p.Ala208LeufsTer15
NM_001251987.2:c.618del NP_001238916.1:p.Ala208LeufsTer15
NM_001256020.2:c.618del NP_001242949.1:p.Ala208LeufsTer15
NM_001256021.2:c.618del NP_001242950.1:p.Ala208LeufsTer15
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