Canonical Allele Identifier: CA3051476086

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691696_97691697insCT , CM000663.2:g.97691696_97691697insCT	GRCh38
NC_000001.10:g.98157252_98157253insCT , CM000663.1:g.98157252_98157253insCT	GRCh37
NC_000001.9:g.97929840_97929841insCT	NCBI36
NG_008807.2:g.234363_234364insAG , LRG_722:g.234363_234364insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+20_762+21insAG MANE Select	ENSP00000359211.3:n.762+20_762+21insAG
ENST00000370192.7:c.762+20_762+21insAG	ENSP00000359211.3:n.762+20_762+21insAG
ENST00000474241.1:n.546_547insAG
NM_000110.3:c.762+20_762+21insAG , LRG_722t1:c.762+20_762+21insAG	NP_000101.2:n.762+20_762+21insAG
XM_005270562.3:c.762+20_762+21insAG	XP_005270619.2:n.762+20_762+21insAG
XM_006710397.2:c.762+20_762+21insAG	XP_006710460.1:n.762+20_762+21insAG
XM_006710397.3:c.762+20_762+21insAG	XP_006710460.1:n.762+20_762+21insAG
XM_017000507.1:c.651+20_651+21insAG	XP_016855996.1:n.651+20_651+21insAG
XM_017000508.2:c.267+20_267+21insAG	XP_016855997.1:n.267+20_267+21insAG
XM_017000509.2:c.267+20_267+21insAG	XP_016855998.1:n.267+20_267+21insAG
XM_017000510.1:c.267+20_267+21insAG	XP_016855999.1:n.267+20_267+21insAG
NM_000110.4:c.762+20_762+21insAG MANE Select	NP_000101.2:n.762+20_762+21insAG