Canonical Allele Identifier: CA3983597

Gene: TRDN

Linked Data

• ClinVar Variation Id: 453105
• ClinVar RCV Id: RCV000523233 ; RCV002525253 ; RCV002420326
• dbSNP Id: rs377368177
• ExAC: 6:123539843 T / C
• gnomAD v2: 6-123539843-T-C
• gnomAD v3: 6-123218698-T-C
• gnomAD v4: 6-123218698-T-C
• MyVariant Identifiers: chr6:g.123539843T>C (hg19) ; chr6:g.123218698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123218698T>C , CM000668.2:g.123218698T>C	GRCh38
NC_000006.11:g.123539843T>C , CM000668.1:g.123539843T>C	GRCh37
NC_000006.10:g.123581542T>C	NCBI36
NG_030438.1:g.423396A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334268.9:c.2093A>G MANE Select	ENSP00000333984.5:p.Asn698Ser
ENST00000334268.8:c.2093A>G	ENSP00000333984.5:p.Asn698Ser
NM_006073.3:c.2093A>G	NP_006064.2:p.Asn698Ser
XM_011535382.1:c.2012A>G	XP_011533684.1:p.Asn671Ser
NM_006073.4:c.2093A>G MANE Select	NP_006064.2:p.Asn698Ser