Canonical Allele Identifier: CA2646709192

Gene: DPYD

Linked Data

• gnomAD v4: 1-97828236-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828236C>A , CM000663.2:g.97828236C>A	GRCh38
NC_000001.10:g.98293792C>A , CM000663.1:g.98293792C>A	GRCh37
NC_000001.9:g.98066380C>A	NCBI36
NG_008807.2:g.97824G>T , LRG_722:g.97824G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.151-40G>T MANE Select	ENSP00000359211.3:n.151-40G>T
ENST00000306031.5:c.151-40G>T	ENSP00000307107.5:n.151-40G>T
ENST00000370192.7:c.151-40G>T	ENSP00000359211.3:n.151-40G>T
NM_000110.3:c.151-40G>T , LRG_722t1:c.151-40G>T	NP_000101.2:n.151-40G>T
NM_001160301.1:c.151-40G>T , LRG_722t2:c.151-40G>T	NP_001153773.1:n.151-40G>T
XM_005270562.3:c.151-40G>T	XP_005270619.2:n.151-40G>T
XM_006710397.2:c.151-40G>T	XP_006710460.1:n.151-40G>T
XM_006710397.3:c.151-40G>T	XP_006710460.1:n.151-40G>T
XM_017000507.1:c.40-40G>T	XP_016855996.1:n.40-40G>T
XM_017000508.2:c.-560-40G>T	XP_016855997.1:n.-560-40G>T
XM_017000509.2:c.-458-40G>T	XP_016855998.1:n.-458-40G>T
XM_017000510.1:c.-458-40G>T	XP_016855999.1:n.-458-40G>T
XR_001737014.1:n.288-40G>T
NM_000110.4:c.151-40G>T MANE Select	NP_000101.2:n.151-40G>T