Canonical Allele Identifier: CA2535136659

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97573694_97573695insC , CM000663.2:g.97573694_97573695insC	GRCh38
NC_000001.10:g.98039250_98039251insC , CM000663.1:g.98039250_98039251insC	GRCh37
NC_000001.9:g.97811838_97811839insC	NCBI36
NG_008807.2:g.352365_352366insG , LRG_722:g.352365_352366insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1339+65_1339+66insG MANE Select	ENSP00000359211.3:n.1339+65_1339+66insG
ENST00000370192.7:c.1339+65_1339+66insG	ENSP00000359211.3:n.1339+65_1339+66insG
NM_000110.3:c.1339+65_1339+66insG , LRG_722t1:c.1339+65_1339+66insG	NP_000101.2:n.1339+65_1339+66insG
XM_005270562.3:c.1339+65_1339+66insG	XP_005270619.2:n.1339+65_1339+66insG
XM_006710397.2:c.1339+65_1339+66insG	XP_006710460.1:n.1339+65_1339+66insG
XM_006710397.3:c.1339+65_1339+66insG	XP_006710460.1:n.1339+65_1339+66insG
XM_017000507.1:c.1228+65_1228+66insG	XP_016855996.1:n.1228+65_1228+66insG
XM_017000508.2:c.844+65_844+66insG	XP_016855997.1:n.844+65_844+66insG
XM_017000509.2:c.844+65_844+66insG	XP_016855998.1:n.844+65_844+66insG
XM_017000510.1:c.844+65_844+66insG	XP_016855999.1:n.844+65_844+66insG
NM_000110.4:c.1339+65_1339+66insG MANE Select	NP_000101.2:n.1339+65_1339+66insG