Canonical Allele Identifier: CA2646705843

Gene: DPYD

Linked Data

• gnomAD v4: 1-97515809-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97515809_97515810insCA , CM000663.2:g.97515809_97515810insCA	GRCh38
NC_000001.10:g.97981365_97981366insCA , CM000663.1:g.97981365_97981366insCA	GRCh37
NC_000001.9:g.97753953_97753954insCA	NCBI36
NG_008807.2:g.410250_410251insTG , LRG_722:g.410250_410251insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1656_1657insTG MANE Select	ENSP00000359211.3:p.Pro553CysfsTer8
ENST00000370192.7:c.1656_1657insTG	ENSP00000359211.3:p.Pro553CysfsTer8
NM_000110.3:c.1656_1657insTG , LRG_722t1:c.1656_1657insTG	NP_000101.2:p.Pro553CysfsTer8
XM_005270562.3:c.1524+33750_1524+33751insTG	XP_005270619.2:n.1524+33750_1524+33751insTG
XM_006710397.2:c.1656_1657insTG	XP_006710460.1:p.Pro553CysfsTer8
XM_006710397.3:c.1656_1657insTG	XP_006710460.1:p.Pro553CysfsTer8
XM_017000507.1:c.1545_1546insTG	XP_016855996.1:p.Pro516CysfsTer8
XM_017000508.2:c.1161_1162insTG	XP_016855997.1:p.Pro388CysfsTer8
XM_017000509.2:c.1161_1162insTG	XP_016855998.1:p.Pro388CysfsTer8
XM_017000510.1:c.1161_1162insTG	XP_016855999.1:p.Pro388CysfsTer8
NM_000110.4:c.1656_1657insTG MANE Select	NP_000101.2:p.Pro553CysfsTer8