Canonical Allele Identifier: CA3983728
Gene: TRDN HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123260632G>A
GRCh37 chr6:g.123581777G>A
Revel Score:
ENST00000398178 0.009
ENST00000398161 0.009
ENST00000334268 (MANE Select) 0.009
gnomAD v2:
6:123581777 G / A
gnomAD v3:
6:123260632 G / A
gnomAD v4:
chr6-123260632-G-A
Joint Max Group AF 0.00043187 (AFR)
Genomes Max Group AF 0.00065534 (AFR)
Exomes Max Group AF 0.00009134 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123260632G>A , CM000668.2:g.123260632G>A GRCh38
NC_000006.11:g.123581777G>A , CM000668.1:g.123581777G>A GRCh37
NC_000006.10:g.123623476G>A NCBI36
NG_030438.1:g.381462C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1811C>T MANE Select ENSP00000333984.5:p.Thr604Ile
ENST00000334268.8:c.1811C>T ENSP00000333984.5:p.Thr604Ile
NM_006073.3:c.1811C>T NP_006064.2:p.Thr604Ile
XM_011535382.1:c.1730C>T XP_011533684.1:p.Thr577Ile
NM_006073.4:c.1811C>T MANE Select NP_006064.2:p.Thr604Ile
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