Canonical Allele Identifier: CA2579225554

Gene: DPYS

Linked Data

• gnomAD v4: 8-104466978-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104466981del , CM000670.2:g.104466981del	GRCh38
NC_000008.10:g.105479209del , CM000670.1:g.105479209del	GRCh37
NC_000008.9:g.105548385del	NCBI36
NG_008840.1:g.5071del
NG_008840.2:g.5071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-59del MANE Select	ENSP00000276651.2:n.-59del
ENST00000351513.6:c.-59del	ENSP00000276651.2:n.-59del
ENST00000521573.2:c.-59del	ENSP00000430246.2:n.-59del
NM_001385.2:c.-59del	NP_001376.1:n.-59del
XM_005250818.2:c.-59del	XP_005250875.1:n.-59del
XM_006716518.2:c.-59del	XP_006716581.1:n.-59del
XM_011516903.1:c.-59del	XP_011515205.1:n.-59del
XM_011516904.1:c.-59del	XP_011515206.1:n.-59del
XR_928507.1:n.112+994del
XM_005250818.3:c.-59del	XP_005250875.1:n.-59del
XM_006716518.3:c.-59del	XP_006716581.1:n.-59del
XM_011516903.3:c.-59del	XP_011515205.1:n.-59del
XM_017013167.2:c.-59del	XP_016868656.1:n.-59del
XM_024447087.1:c.-59del	XP_024302855.1:n.-59del
XR_001745489.1:n.96del
XR_001745490.2:n.96del
XR_928507.2:n.233+994del
NM_001385.3:c.-59del MANE Select	NP_001376.1:n.-59del