Canonical Allele Identifier: CA419145321

Gene: DPYD

Linked Data

• dbSNP Id: rs1366312698
• gnomAD v3: 1-97450031-CTT-C
• gnomAD v4: 1-97450031-CTT-C
• MyVariant Identifiers: chr1:g.97915588_97915589del (hg19) ; chr1:g.97450032_97450033del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450032_97450033del , CM000663.2:g.97450032_97450033del	GRCh38
NC_000001.10:g.97915588_97915589del , CM000663.1:g.97915588_97915589del	GRCh37
NC_000001.9:g.97688176_97688177del	NCBI36
NG_008807.2:g.476027_476028del , LRG_722:g.476027_476028del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+26_1905+27del MANE Select	ENSP00000359211.3:n.1905+26_1905+27del
ENST00000370192.7:c.1905+26_1905+27del	ENSP00000359211.3:n.1905+26_1905+27del
NM_000110.3:c.1905+26_1905+27del , LRG_722t1:c.1905+26_1905+27del	NP_000101.2:n.1905+26_1905+27del
XM_005270562.3:c.1689+26_1689+27del	XP_005270619.2:n.1689+26_1689+27del
XM_006710397.2:c.1905+26_1905+27del	XP_006710460.1:n.1905+26_1905+27del
XM_006710397.3:c.1905+26_1905+27del	XP_006710460.1:n.1905+26_1905+27del
XM_017000507.1:c.1794+26_1794+27del	XP_016855996.1:n.1794+26_1794+27del
XM_017000508.2:c.1410+26_1410+27del	XP_016855997.1:n.1410+26_1410+27del
XM_017000509.2:c.1410+26_1410+27del	XP_016855998.1:n.1410+26_1410+27del
XM_017000510.1:c.1410+26_1410+27del	XP_016855999.1:n.1410+26_1410+27del
NM_000110.4:c.1905+26_1905+27del MANE Select	NP_000101.2:n.1905+26_1905+27del