Canonical Allele Identifier: CA844980514

Gene: DPYS

Linked Data

• dbSNP Id: rs1471870798
• MyVariant Identifiers: chr8:g.105479164G>A (hg19) ; chr8:g.104466936G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104466936G>A , CM000670.2:g.104466936G>A	GRCh38
NC_000008.10:g.105479164G>A , CM000670.1:g.105479164G>A	GRCh37
NC_000008.9:g.105548340G>A	NCBI36
NG_008840.1:g.5114C>T
NG_008840.2:g.5114C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-16C>T MANE Select	ENSP00000276651.2:n.-16C>T
ENST00000351513.6:c.-16C>T	ENSP00000276651.2:n.-16C>T
ENST00000521573.2:c.-16C>T	ENSP00000430246.2:n.-16C>T
NM_001385.2:c.-16C>T	NP_001376.1:n.-16C>T
XM_005250818.2:c.-16C>T	XP_005250875.1:n.-16C>T
XM_006716518.2:c.-16C>T	XP_006716581.1:n.-16C>T
XM_011516903.1:c.-16C>T	XP_011515205.1:n.-16C>T
XM_011516904.1:c.-16C>T	XP_011515206.1:n.-16C>T
XR_928507.1:n.112+949G>A
XM_005250818.3:c.-16C>T	XP_005250875.1:n.-16C>T
XM_006716518.3:c.-16C>T	XP_006716581.1:n.-16C>T
XM_011516903.3:c.-16C>T	XP_011515205.1:n.-16C>T
XM_017013167.2:c.-16C>T	XP_016868656.1:n.-16C>T
XM_024447087.1:c.-16C>T	XP_024302855.1:n.-16C>T
XR_001745489.1:n.139C>T
XR_001745490.2:n.139C>T
XR_928507.2:n.233+949G>A
NM_001385.3:c.-16C>T MANE Select	NP_001376.1:n.-16C>T