Canonical Allele Identifier: CA2646711309

Gene: DPYD

Linked Data

• gnomAD v4: 1-97883175-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97883175C>T , CM000663.2:g.97883175C>T	GRCh38
NC_000001.10:g.98348731C>T , CM000663.1:g.98348731C>T	GRCh37
NC_000001.9:g.98121319C>T	NCBI36
NG_008807.2:g.42885G>A , LRG_722:g.42885G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.150+89G>A MANE Select	ENSP00000359211.3:n.150+89G>A
ENST00000306031.5:c.150+89G>A	ENSP00000307107.5:n.150+89G>A
ENST00000370192.7:c.150+89G>A	ENSP00000359211.3:n.150+89G>A
ENST00000460019.1:n.225+89G>A
NM_000110.3:c.150+89G>A , LRG_722t1:c.150+89G>A	NP_000101.2:n.150+89G>A
NM_001160301.1:c.150+89G>A , LRG_722t2:c.150+89G>A	NP_001153773.1:n.150+89G>A
XM_005270562.3:c.150+89G>A	XP_005270619.2:n.150+89G>A
XM_006710397.2:c.150+89G>A	XP_006710460.1:n.150+89G>A
XM_006710397.3:c.150+89G>A	XP_006710460.1:n.150+89G>A
XM_017000507.1:c.39+37709G>A	XP_016855996.1:n.39+37709G>A
XM_017000508.2:c.-561+89G>A	XP_016855997.1:n.-561+89G>A
XM_017000509.2:c.-459+89G>A	XP_016855998.1:n.-459+89G>A
XM_017000510.1:c.-459+37709G>A	XP_016855999.1:n.-459+37709G>A
XR_001737014.1:n.287+89G>A
NM_000110.4:c.150+89G>A MANE Select	NP_000101.2:n.150+89G>A