Canonical Allele Identifier: CA3983584

Gene: TRDN

Linked Data

• ClinVar Variation Id: 408735
• ClinVar RCV Id: RCV002429506 ; RCV002525570
• dbSNP Id: rs768748530
• ExAC: 6:123539793 T / C
• gnomAD v2: 6-123539793-T-C
• gnomAD v3: 6-123218648-T-C
• gnomAD v4: 6-123218648-T-C
• COSMIC: COSM5507133
• MyVariant Identifiers: chr6:g.123539793T>C (hg19) ; chr6:g.123218648T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218648T>C , CM000668.2:g.123218648T>C	GRCh38
NC_000006.11:g.123539793T>C , CM000668.1:g.123539793T>C	GRCh37
NC_000006.10:g.123581492T>C	NCBI36
NG_030438.1:g.423446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2143A>G MANE Select	ENSP00000333984.5:p.Ser715Gly
ENST00000334268.8:c.2143A>G	ENSP00000333984.5:p.Ser715Gly
NM_006073.3:c.2143A>G	NP_006064.2:p.Ser715Gly
XM_011535382.1:c.2062A>G	XP_011533684.1:p.Ser688Gly
NM_006073.4:c.2143A>G MANE Select	NP_006064.2:p.Ser715Gly