Canonical Allele Identifier: CA3983705
Gene: TRDN HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123255878C>T
GRCh37 chr6:g.123577023C>T
Revel Score:
ENST00000398178 0.011
ENST00000398161 0.011
ENST00000334268 (MANE Select) 0.011
gnomAD v2:
6:123577023 C / T
gnomAD v3:
6:123255878 C / T
gnomAD v4:
chr6-123255878-C-T
Joint Max Group AF 0.00098967 (AFR)
Genomes Max Group AF 0.00095877 (AFR)
Exomes Max Group AF 0.00082177 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123255878C>T , CM000668.2:g.123255878C>T GRCh38
NC_000006.11:g.123577023C>T , CM000668.1:g.123577023C>T GRCh37
NC_000006.10:g.123618722C>T NCBI36
NG_030438.1:g.386216G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1895G>A MANE Select ENSP00000333984.5:p.Arg632Lys
ENST00000334268.8:c.1895G>A ENSP00000333984.5:p.Arg632Lys
NM_006073.3:c.1895G>A NP_006064.2:p.Arg632Lys
XM_011535382.1:c.1814G>A XP_011533684.1:p.Arg605Lys
NM_006073.4:c.1895G>A MANE Select NP_006064.2:p.Arg632Lys
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