Canonical Allele Identifier: CA3983590

Gene: TRDN

Linked Data

• ClinVar Variation Id: 240286
• ClinVar RCV Id: RCV001658061 ; RCV002418016 ; RCV002519797
• dbSNP Id: rs373408498
• ExAC: 6:123539805 G / A
• gnomAD v2: 6-123539805-G-A
• gnomAD v3: 6-123218660-G-A
• gnomAD v4: 6-123218660-G-A
• MyVariant Identifiers: chr6:g.123539805G>A (hg19) ; chr6:g.123218660G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218660G>A , CM000668.2:g.123218660G>A	GRCh38
NC_000006.11:g.123539805G>A , CM000668.1:g.123539805G>A	GRCh37
NC_000006.10:g.123581504G>A	NCBI36
NG_030438.1:g.423434C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2131C>T MANE Select	ENSP00000333984.5:p.Arg711Cys
ENST00000334268.8:c.2131C>T	ENSP00000333984.5:p.Arg711Cys
NM_006073.3:c.2131C>T	NP_006064.2:p.Arg711Cys
XM_011535382.1:c.2050C>T	XP_011533684.1:p.Arg684Cys
NM_006073.4:c.2131C>T MANE Select	NP_006064.2:p.Arg711Cys