Canonical Allele Identifier: CA740802033

Gene: DPYD

Linked Data

• dbSNP Id: rs1438641113
• gnomAD v3: 1-97357301-CATT-C
• gnomAD v4: 1-97357301-CATT-C
• MyVariant Identifiers: chr1:g.97822858_97822860del (hg19) ; chr1:g.97357302_97357304del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97357302_97357304del , CM000663.2:g.97357302_97357304del	GRCh38
NC_000001.10:g.97822858_97822860del , CM000663.1:g.97822858_97822860del	GRCh37
NC_000001.9:g.97595446_97595448del	NCBI36
NG_008807.2:g.568756_568758del , LRG_722:g.568756_568758del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2058+16257_2058+16259del MANE Select	ENSP00000359211.3:n.2058+16257_2058+16259del
ENST00000370192.7:c.2058+16257_2058+16259del	ENSP00000359211.3:n.2058+16257_2058+16259del
NM_000110.3:c.2058+16257_2058+16259del , LRG_722t1:c.2058+16257_2058+16259del	NP_000101.2:n.2058+16257_2058+16259del
XM_005270562.3:c.1842+16257_1842+16259del	XP_005270619.2:n.1842+16257_1842+16259del
XM_006710397.2:c.2058+16257_2058+16259del	XP_006710460.1:n.2058+16257_2058+16259del
XR_947619.1:n.921-9696_921-9694del
XR_947620.1:n.921-9696_921-9694del
XR_947621.1:n.921-9696_921-9694del
XM_006710397.3:c.2058+16257_2058+16259del	XP_006710460.1:n.2058+16257_2058+16259del
XM_017000507.1:c.1947+16257_1947+16259del	XP_016855996.1:n.1947+16257_1947+16259del
XM_017000508.2:c.1563+16257_1563+16259del	XP_016855997.1:n.1563+16257_1563+16259del
XM_017000509.2:c.1563+16257_1563+16259del	XP_016855998.1:n.1563+16257_1563+16259del
XM_017000510.1:c.1563+16257_1563+16259del	XP_016855999.1:n.1563+16257_1563+16259del
NM_000110.4:c.2058+16257_2058+16259del MANE Select	NP_000101.2:n.2058+16257_2058+16259del