Canonical Allele Identifier: CA2561026408

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691194_97691195insT , CM000663.2:g.97691194_97691195insT	GRCh38
NC_000001.10:g.98156750_98156751insT , CM000663.1:g.98156750_98156751insT	GRCh37
NC_000001.9:g.97929338_97929339insT	NCBI36
NG_008807.2:g.234865_234866insA , LRG_722:g.234865_234866insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+522_762+523insA MANE Select	ENSP00000359211.3:n.762+522_762+523insA
ENST00000370192.7:c.762+522_762+523insA	ENSP00000359211.3:n.762+522_762+523insA
NM_000110.3:c.762+522_762+523insA , LRG_722t1:c.762+522_762+523insA	NP_000101.2:n.762+522_762+523insA
XM_005270562.3:c.762+522_762+523insA	XP_005270619.2:n.762+522_762+523insA
XM_006710397.2:c.762+522_762+523insA	XP_006710460.1:n.762+522_762+523insA
XM_006710397.3:c.762+522_762+523insA	XP_006710460.1:n.762+522_762+523insA
XM_017000507.1:c.651+522_651+523insA	XP_016855996.1:n.651+522_651+523insA
XM_017000508.2:c.267+522_267+523insA	XP_016855997.1:n.267+522_267+523insA
XM_017000509.2:c.267+522_267+523insA	XP_016855998.1:n.267+522_267+523insA
XM_017000510.1:c.267+522_267+523insA	XP_016855999.1:n.267+522_267+523insA
NM_000110.4:c.762+522_762+523insA MANE Select	NP_000101.2:n.762+522_762+523insA