Canonical Allele Identifier: CA2841054689

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104467015C>A , CM000670.2:g.104467015C>A	GRCh38
NC_000008.10:g.105479243C>A , CM000670.1:g.105479243C>A	GRCh37
NC_000008.9:g.105548419C>A	NCBI36
NG_008840.1:g.5035G>T
NG_008840.2:g.5035G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-95G>T MANE Select	ENSP00000276651.2:n.-95G>T
ENST00000351513.6:c.-95G>T	ENSP00000276651.2:n.-95G>T
ENST00000521573.2:c.-95G>T	ENSP00000430246.2:n.-95G>T
NM_001385.2:c.-95G>T	NP_001376.1:n.-95G>T
XM_005250818.2:c.-95G>T	XP_005250875.1:n.-95G>T
XM_006716518.2:c.-95G>T	XP_006716581.1:n.-95G>T
XM_011516903.1:c.-95G>T	XP_011515205.1:n.-95G>T
XM_011516904.1:c.-95G>T	XP_011515206.1:n.-95G>T
XR_928507.1:n.112+1028C>A
XM_005250818.3:c.-95G>T	XP_005250875.1:n.-95G>T
XM_006716518.3:c.-95G>T	XP_006716581.1:n.-95G>T
XM_011516903.3:c.-95G>T	XP_011515205.1:n.-95G>T
XM_017013167.2:c.-95G>T	XP_016868656.1:n.-95G>T
XM_024447087.1:c.-95G>T	XP_024302855.1:n.-95G>T
XR_001745489.1:n.60G>T
XR_001745490.2:n.60G>T
XR_928507.2:n.233+1028C>A
NM_001385.3:c.-95G>T MANE Select	NP_001376.1:n.-95G>T