Canonical Allele Identifier: CA3984230
Gene: TRDN HGNC NCBI
TRDN-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123464953G>A
GRCh37 chr6:g.123786098G>A
Revel Score:
ENST00000398178 0.036
ENST00000398161 0.036
ENST00000334268 (MANE Select) 0.036
ENST00000542014 0.036
ENST00000543022 0.036
ENST00000546248 0.036
gnomAD v2:
6:123786098 G / A
gnomAD v3:
6:123464953 G / A
gnomAD v4:
chr6-123464953-G-A
Joint Max Group AF 0.00011887 (NFE)
Genomes Max Group AF 0.00004768 (NFE)
Exomes Max Group AF 0.0001203 (NFE)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123464953G>A , CM000668.2:g.123464953G>A GRCh38
NC_000006.11:g.123786098G>A , CM000668.1:g.123786098G>A GRCh37
NC_000006.10:g.123827797G>A NCBI36
NG_030438.1:g.177141C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.884C>T (TRDN) MANE Select ENSP00000333984.5:p.Pro295Leu
ENST00000662930.1:c.884C>T (TRDN) ENSP00000499585.1:p.Pro295Leu
ENST00000334268.8:c.884C>T (TRDN) ENSP00000333984.5:p.Pro295Leu
ENST00000628709.2:c.824C>T (TRDN) ENSP00000486095.1:p.Pro275Leu
NM_001251987.1:c.884C>T (TRDN) NP_001238916.1:p.Pro295Leu
NM_001256020.1:c.824C>T (TRDN) NP_001242949.1:p.Pro275Leu
NM_006073.3:c.884C>T (TRDN) NP_006064.2:p.Pro295Leu
NR_110844.1:n.175-3863G>A (TRDN-AS1)
XM_011535382.1:c.884C>T (TRDN) XP_011533684.1:p.Pro295Leu
NM_006073.4:c.884C>T (TRDN) MANE Select NP_006064.2:p.Pro295Leu
NM_001251987.2:c.884C>T (TRDN) NP_001238916.1:p.Pro295Leu
NM_001256020.2:c.824C>T (TRDN) NP_001242949.1:p.Pro275Leu
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