Canonical Allele Identifier: CA1004794310

Gene: DPYD

Linked Data

• dbSNP Id: rs1660991738
• gnomAD v3: 1-97691195-AT-A
• gnomAD v4: 1-97691195-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691196del , CM000663.2:g.97691196del	GRCh38
NC_000001.10:g.98156752del , CM000663.1:g.98156752del	GRCh37
NC_000001.9:g.97929340del	NCBI36
NG_008807.2:g.234864del , LRG_722:g.234864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+521del MANE Select	ENSP00000359211.3:n.762+521del
ENST00000370192.7:c.762+521del	ENSP00000359211.3:n.762+521del
NM_000110.3:c.762+521del , LRG_722t1:c.762+521del	NP_000101.2:n.762+521del
XM_005270562.3:c.762+521del	XP_005270619.2:n.762+521del
XM_006710397.2:c.762+521del	XP_006710460.1:n.762+521del
XM_006710397.3:c.762+521del	XP_006710460.1:n.762+521del
XM_017000507.1:c.651+521del	XP_016855996.1:n.651+521del
XM_017000508.2:c.267+521del	XP_016855997.1:n.267+521del
XM_017000509.2:c.267+521del	XP_016855998.1:n.267+521del
XM_017000510.1:c.267+521del	XP_016855999.1:n.267+521del
NM_000110.4:c.762+521del MANE Select	NP_000101.2:n.762+521del