Canonical Allele Identifier: CA3984382

Gene: TRDN

Linked Data

• ClinVar Variation Id: 227121
• ClinVar RCV Id: RCV000213504 ; RCV001572730 ; RCV002519599 ; RCV003741164 ; RCV000618354 ; RCV003977606
• dbSNP Id: rs79182520
• ExAC: 6:123851705 G / A
• gnomAD v2: 6-123851705-G-A
• gnomAD v3: 6-123530560-G-A
• gnomAD v4: 6-123530560-G-A
• MyVariant Identifiers: chr6:g.123851705G>A (hg19) ; chr6:g.123530560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123530560G>A , CM000668.2:g.123530560G>A	GRCh38
NC_000006.11:g.123851705G>A , CM000668.1:g.123851705G>A	GRCh37
NC_000006.10:g.123893404G>A	NCBI36
NG_030438.1:g.111534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361029.9:c.232C>T	ENSP00000354307.5:p.His78Tyr
ENST00000422596.2:c.232C>T	ENSP00000406768.2:p.His78Tyr
ENST00000546248.6:c.430C>T	ENSP00000439281.2:p.His144Tyr
ENST00000334268.9:c.430C>T MANE Select	ENSP00000333984.5:p.His144Tyr
ENST00000662930.1:c.430C>T	ENSP00000499585.1:p.His144Tyr
ENST00000334268.8:c.430C>T	ENSP00000333984.5:p.His144Tyr
ENST00000422596.1:c.6C>T
ENST00000542443.5:c.430C>T	ENSP00000437684.1:p.His144Tyr
ENST00000546248.5:c.430C>T	ENSP00000439281.2:p.His144Tyr
ENST00000628709.2:c.430C>T	ENSP00000486095.1:p.His144Tyr
NM_001251987.1:c.430C>T	NP_001238916.1:p.His144Tyr
NM_001256020.1:c.430C>T	NP_001242949.1:p.His144Tyr
NM_001256021.1:c.430C>T	NP_001242950.1:p.His144Tyr
NM_001256022.1:c.430C>T	NP_001242951.1:p.His144Tyr
NM_006073.3:c.430C>T	NP_006064.2:p.His144Tyr
XM_011535382.1:c.430C>T	XP_011533684.1:p.His144Tyr
XR_942945.1:n.2171-1046G>A
XR_001743833.1:n.1960-1046G>A
NM_006073.4:c.430C>T MANE Select	NP_006064.2:p.His144Tyr
NM_001251987.2:c.430C>T	NP_001238916.1:p.His144Tyr
NM_001256020.2:c.430C>T	NP_001242949.1:p.His144Tyr
NM_001256021.2:c.430C>T	NP_001242950.1:p.His144Tyr
NM_001256022.2:c.430C>T	NP_001242951.1:p.His144Tyr