Canonical Allele Identifier: CA1182873363

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97449907_97449912delinsCTTTTT , CM000663.2:g.97449907_97449912delinsCTTTTT	GRCh38
NC_000001.10:g.97915463_97915468delinsCTTTTT , CM000663.1:g.97915463_97915468delinsCTTTTT	GRCh37
NC_000001.9:g.97688051_97688056delinsCTTTTT	NCBI36
NG_008807.2:g.476148_476153delinsAAAAAG , LRG_722:g.476148_476153delinsAAAAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+147_1905+152delinsAAAAAG MANE Select	ENSP00000359211.3:n.1905+147_1905+152delinsAAAAAG
ENST00000370192.7:c.1905+147_1905+152delinsAAAAAG	ENSP00000359211.3:n.1905+147_1905+152delinsAAAAAG
NM_000110.3:c.1905+147_1905+152delinsAAAAAG , LRG_722t1:c.1905+147_1905+152delinsAAAAAG	NP_000101.2:n.1905+147_1905+152delinsAAAAAG
XM_005270562.3:c.1689+147_1689+152delinsAAAAAG	XP_005270619.2:n.1689+147_1689+152delinsAAAAAG
XM_006710397.2:c.1905+147_1905+152delinsAAAAAG	XP_006710460.1:n.1905+147_1905+152delinsAAAAAG
XM_006710397.3:c.1905+147_1905+152delinsAAAAAG	XP_006710460.1:n.1905+147_1905+152delinsAAAAAG
XM_017000507.1:c.1794+147_1794+152delinsAAAAAG	XP_016855996.1:n.1794+147_1794+152delinsAAAAAG
XM_017000508.2:c.1410+147_1410+152delinsAAAAAG	XP_016855997.1:n.1410+147_1410+152delinsAAAAAG
XM_017000509.2:c.1410+147_1410+152delinsAAAAAG	XP_016855998.1:n.1410+147_1410+152delinsAAAAAG
XM_017000510.1:c.1410+147_1410+152delinsAAAAAG	XP_016855999.1:n.1410+147_1410+152delinsAAAAAG
NM_000110.4:c.1905+147_1905+152delinsAAAAAG MANE Select	NP_000101.2:n.1905+147_1905+152delinsAAAAAG