Canonical Allele Identifier: CA3983730
Gene: TRDN HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123260635C>G
GRCh37 chr6:g.123581780C>G
Revel Score:
ENST00000398178 0.002
ENST00000398161 0.002
ENST00000334268 (MANE Select) 0.002
gnomAD v2:
6:123581780 C / G
gnomAD v3:
6:123260635 C / G
gnomAD v4:
chr6-123260635-C-G
Joint Max Group AF 0.00001848 (NFE)
Genomes Max Group AF 0.00008224 (NFE)
Exomes Max Group AF 0.00001276 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123260635C>G , CM000668.2:g.123260635C>G GRCh38
NC_000006.11:g.123581780C>G , CM000668.1:g.123581780C>G GRCh37
NC_000006.10:g.123623479C>G NCBI36
NG_030438.1:g.381459G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1808G>C MANE Select ENSP00000333984.5:p.Gly603Ala
ENST00000334268.8:c.1808G>C ENSP00000333984.5:p.Gly603Ala
NM_006073.3:c.1808G>C NP_006064.2:p.Gly603Ala
XM_011535382.1:c.1727G>C XP_011533684.1:p.Gly576Ala
NM_006073.4:c.1808G>C MANE Select NP_006064.2:p.Gly603Ala
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