Canonical Allele Identifier: CA1182717102

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098309_97098310delinsTA , CM000663.2:g.97098309_97098310delinsTA	GRCh38
NC_000001.10:g.97563865_97563866delinsTA , CM000663.1:g.97563865_97563866delinsTA	GRCh37
NC_000001.9:g.97336453_97336454delinsTA	NCBI36
NG_008807.2:g.827750_827751delinsTA , LRG_722:g.827750_827751delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2766+179_2766+180delinsTA (DPYD) MANE Select	ENSP00000359211.3:n.2766+179_2766+180delinsTA
ENST00000370192.7:c.2766+179_2766+180delinsTA (DPYD)	ENSP00000359211.3:n.2766+179_2766+180delinsTA
NM_000110.3:c.2766+179_2766+180delinsTA , LRG_722t1:c.2766+179_2766+180delinsTA (DPYD)	NP_000101.2:n.2766+179_2766+180delinsTA
NR_046590.1:n.64+2323_64+2324delinsTA (DPYD-AS1)
XM_005270562.3:c.2550+179_2550+180delinsTA (DPYD)	XP_005270619.2:n.2550+179_2550+180delinsTA
XM_017000507.1:c.2655+179_2655+180delinsTA (DPYD)	XP_016855996.1:n.2655+179_2655+180delinsTA
XM_017000508.2:c.2271+179_2271+180delinsTA (DPYD)	XP_016855997.1:n.2271+179_2271+180delinsTA
XM_017000509.2:c.2271+179_2271+180delinsTA (DPYD)	XP_016855998.1:n.2271+179_2271+180delinsTA
XM_017000510.1:c.2271+179_2271+180delinsTA (DPYD)	XP_016855999.1:n.2271+179_2271+180delinsTA
NM_000110.4:c.2766+179_2766+180delinsTA (DPYD) MANE Select	NP_000101.2:n.2766+179_2766+180delinsTA