Canonical Allele Identifier: CA1182873429

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450065_97450066delinsTG , CM000663.2:g.97450065_97450066delinsTG	GRCh38
NC_000001.10:g.97915621_97915622delinsTG , CM000663.1:g.97915621_97915622delinsTG	GRCh37
NC_000001.9:g.97688209_97688210delinsTG	NCBI36
NG_008807.2:g.475994_475995delinsCA , LRG_722:g.475994_475995delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1898_1899delinsCA MANE Select	ENSP00000359211.3:p.Pro633=
ENST00000370192.7:c.1898_1899delinsCA	ENSP00000359211.3:p.Pro633=
NM_000110.3:c.1898_1899delinsCA , LRG_722t1:c.1898_1899delinsCA	NP_000101.2:p.Pro633=
XM_005270562.3:c.1682_1683delinsCA	XP_005270619.2:p.Pro561=
XM_006710397.2:c.1898_1899delinsCA	XP_006710460.1:p.Pro633=
XM_006710397.3:c.1898_1899delinsCA	XP_006710460.1:p.Pro633=
XM_017000507.1:c.1787_1788delinsCA	XP_016855996.1:p.Pro596=
XM_017000508.2:c.1403_1404delinsCA	XP_016855997.1:p.Pro468=
XM_017000509.2:c.1403_1404delinsCA	XP_016855998.1:p.Pro468=
XM_017000510.1:c.1403_1404delinsCA	XP_016855999.1:p.Pro468=
NM_000110.4:c.1898_1899delinsCA MANE Select	NP_000101.2:p.Pro633=