Canonical Allele Identifier: CA2580856398

Gene: DCSTAMP DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104347204C>A , CM000670.2:g.104347204C>A	GRCh38
NC_000008.10:g.105359432C>A , CM000670.1:g.105359432C>A	GRCh37
NC_000008.9:g.105428608C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297581.2:c.-12-1337C>A (DCSTAMP) MANE Select	ENSP00000297581.2:n.-12-1337C>A
ENST00000517364.1:n.330-1337C>A (DCSTAMP)
ENST00000518023.5:n.192-1337C>A (DCSTAMP)
ENST00000519562.1:n.437-1337C>A (DCSTAMP)
ENST00000521601.1:n.329-15240G>T (DPYS)
ENST00000622554.1:c.-12-1337C>A (DCSTAMP)	ENSP00000480546.1:n.-12-1337C>A
NM_001257317.1:c.-12-1337C>A (DCSTAMP)	NP_001244246.1:n.-12-1337C>A
NM_030788.3:c.-12-1337C>A (DCSTAMP)	NP_110415.1:n.-12-1337C>A
XM_005251075.1:c.-12-1337C>A (DCSTAMP)	XP_005251132.1:n.-12-1337C>A
XM_011517321.1:c.-12-1337C>A (DCSTAMP)	XP_011515623.1:n.-12-1337C>A
XM_011517322.1:c.-12-1337C>A (DCSTAMP)	XP_011515624.1:n.-12-1337C>A
XM_011517323.1:c.-12-1337C>A (DCSTAMP)	XP_011515625.1:n.-12-1337C>A
XM_011517324.1:c.-12-1337C>A (DCSTAMP)	XP_011515626.1:n.-12-1337C>A
XM_024447288.1:c.-12-1337C>A (DCSTAMP)	XP_024303056.1:n.-12-1337C>A
XM_024447289.1:c.-12-1337C>A (DCSTAMP)	XP_024303057.1:n.-12-1337C>A
XM_024447290.1:c.-12-1337C>A (DCSTAMP)	XP_024303058.1:n.-12-1337C>A
NM_030788.4:c.-12-1337C>A (DCSTAMP) MANE Select	NP_110415.1:n.-12-1337C>A