Canonical Allele Identifier: CA182641814

Gene: DPYS

Linked Data

• dbSNP Id: rs970515000
• gnomAD v3: 8-104466999-G-T
• gnomAD v4: 8-104466999-G-T
• MyVariant Identifiers: chr8:g.105479227G>T (hg19) ; chr8:g.104466999G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104466999G>T , CM000670.2:g.104466999G>T	GRCh38
NC_000008.10:g.105479227G>T , CM000670.1:g.105479227G>T	GRCh37
NC_000008.9:g.105548403G>T	NCBI36
NG_008840.1:g.5051C>A
NG_008840.2:g.5051C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-79C>A MANE Select	ENSP00000276651.2:n.-79C>A
ENST00000351513.6:c.-79C>A	ENSP00000276651.2:n.-79C>A
ENST00000521573.2:c.-79C>A	ENSP00000430246.2:n.-79C>A
NM_001385.2:c.-79C>A	NP_001376.1:n.-79C>A
XM_005250818.2:c.-79C>A	XP_005250875.1:n.-79C>A
XM_006716518.2:c.-79C>A	XP_006716581.1:n.-79C>A
XM_011516903.1:c.-79C>A	XP_011515205.1:n.-79C>A
XM_011516904.1:c.-79C>A	XP_011515206.1:n.-79C>A
XR_928507.1:n.112+1012G>T
XM_005250818.3:c.-79C>A	XP_005250875.1:n.-79C>A
XM_006716518.3:c.-79C>A	XP_006716581.1:n.-79C>A
XM_011516903.3:c.-79C>A	XP_011515205.1:n.-79C>A
XM_017013167.2:c.-79C>A	XP_016868656.1:n.-79C>A
XM_024447087.1:c.-79C>A	XP_024302855.1:n.-79C>A
XR_001745489.1:n.76C>A
XR_001745490.2:n.76C>A
XR_928507.2:n.233+1012G>T
NM_001385.3:c.-79C>A MANE Select	NP_001376.1:n.-79C>A