Canonical Allele Identifier: CA3983801
Gene: TRDN HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123271146T>G
GRCh37 chr6:g.123592291T>G
Revel Score:
ENST00000398178 0.087
ENST00000398161 0.087
ENST00000334268 (MANE Select) 0.087
gnomAD v2:
6:123592291 T / G
gnomAD v3:
6:123271146 T / G
gnomAD v4:
chr6-123271146-T-G
Joint Max Group AF 0.00410785 (AFR)
Genomes Max Group AF 0.00404333 (AFR)
Exomes Max Group AF 0.00381938 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123271146T>G , CM000668.2:g.123271146T>G GRCh38
NC_000006.11:g.123592291T>G , CM000668.1:g.123592291T>G GRCh37
NC_000006.10:g.123633990T>G NCBI36
NG_030438.1:g.370948A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1713A>C MANE Select ENSP00000333984.5:p.Glu571Asp
ENST00000334268.8:c.1713A>C ENSP00000333984.5:p.Glu571Asp
NM_006073.3:c.1713A>C NP_006064.2:p.Glu571Asp
XM_011535382.1:c.1632A>C XP_011533684.1:p.Glu544Asp
NM_006073.4:c.1713A>C MANE Select NP_006064.2:p.Glu571Asp
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