Canonical Allele Identifier: CA2646705578

Gene: DPYD

Linked Data

• gnomAD v4: 1-97450108-G-GCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450109_97450110insTTC , CM000663.2:g.97450109_97450110insTTC	GRCh38
NC_000001.10:g.97915665_97915666insTTC , CM000663.1:g.97915665_97915666insTTC	GRCh37
NC_000001.9:g.97688253_97688254insTTC	NCBI36
NG_008807.2:g.475951_475952insAAG , LRG_722:g.475951_475952insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1855_1856insAAG MANE Select	ENSP00000359211.3:p.Ala618_Ala619insGlu
ENST00000370192.7:c.1855_1856insAAG	ENSP00000359211.3:p.Ala618_Ala619insGlu
NM_000110.3:c.1855_1856insAAG , LRG_722t1:c.1855_1856insAAG	NP_000101.2:p.Ala618_Ala619insGlu
XM_005270562.3:c.1639_1640insAAG	XP_005270619.2:p.Ala546_Ala547insGlu
XM_006710397.2:c.1855_1856insAAG	XP_006710460.1:p.Ala618_Ala619insGlu
XM_006710397.3:c.1855_1856insAAG	XP_006710460.1:p.Ala618_Ala619insGlu
XM_017000507.1:c.1744_1745insAAG	XP_016855996.1:p.Ala581_Ala582insGlu
XM_017000508.2:c.1360_1361insAAG	XP_016855997.1:p.Ala453_Ala454insGlu
XM_017000509.2:c.1360_1361insAAG	XP_016855998.1:p.Ala453_Ala454insGlu
XM_017000510.1:c.1360_1361insAAG	XP_016855999.1:p.Ala453_Ala454insGlu
NM_000110.4:c.1855_1856insAAG MANE Select	NP_000101.2:p.Ala618_Ala619insGlu