Canonical Allele Identifier: CA740814676

Gene: DPYD

Linked Data

• dbSNP Id: rs1193321121
• gnomAD v3: 1-97382570-AG-A
• gnomAD v4: 1-97382570-AG-A
• MyVariant Identifiers: chr1:g.97848127del (hg19) ; chr1:g.97382571del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382571del , CM000663.2:g.97382571del	GRCh38
NC_000001.10:g.97848127del , CM000663.1:g.97848127del	GRCh37
NC_000001.9:g.97620715del	NCBI36
NG_008807.2:g.543489del , LRG_722:g.543489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-110del MANE Select	ENSP00000359211.3:n.1906-110del
ENST00000370192.7:c.1906-110del	ENSP00000359211.3:n.1906-110del
NM_000110.3:c.1906-110del , LRG_722t1:c.1906-110del	NP_000101.2:n.1906-110del
XM_005270562.3:c.1690-110del	XP_005270619.2:n.1690-110del
XM_006710397.2:c.1906-110del	XP_006710460.1:n.1906-110del
XR_947619.1:n.1347-1063del
XR_947620.1:n.1125-1063del
XR_947621.1:n.1347-1063del
XM_006710397.3:c.1906-110del	XP_006710460.1:n.1906-110del
XM_017000507.1:c.1795-110del	XP_016855996.1:n.1795-110del
XM_017000508.2:c.1411-110del	XP_016855997.1:n.1411-110del
XM_017000509.2:c.1411-110del	XP_016855998.1:n.1411-110del
XM_017000510.1:c.1411-110del	XP_016855999.1:n.1411-110del
XR_001737686.2:n.692-1063del
XR_001737687.1:n.692-1063del
XR_001737688.2:n.692-1063del
NM_000110.4:c.1906-110del MANE Select	NP_000101.2:n.1906-110del