Canonical Allele Identifier: CA1182717295

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098820_97098821delinsTA , CM000663.2:g.97098820_97098821delinsTA	GRCh38
NC_000001.10:g.97564376_97564377delinsTA , CM000663.1:g.97564376_97564377delinsTA	GRCh37
NC_000001.9:g.97336964_97336965delinsTA	NCBI36
NG_008807.2:g.827239_827240delinsTA , LRG_722:g.827239_827240delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-189_2623-188delinsTA (DPYD) MANE Select	ENSP00000359211.3:n.2623-189_2623-188delinsTA
ENST00000370192.7:c.2623-189_2623-188delinsTA (DPYD)	ENSP00000359211.3:n.2623-189_2623-188delinsTA
NM_000110.3:c.2623-189_2623-188delinsTA , LRG_722t1:c.2623-189_2623-188delinsTA (DPYD)	NP_000101.2:n.2623-189_2623-188delinsTA
NR_046590.1:n.64+2834_64+2835delinsTA (DPYD-AS1)
XM_005270562.3:c.2407-189_2407-188delinsTA (DPYD)	XP_005270619.2:n.2407-189_2407-188delinsTA
XM_017000507.1:c.2512-189_2512-188delinsTA (DPYD)	XP_016855996.1:n.2512-189_2512-188delinsTA
XM_017000508.2:c.2128-189_2128-188delinsTA (DPYD)	XP_016855997.1:n.2128-189_2128-188delinsTA
XM_017000509.2:c.2128-189_2128-188delinsTA (DPYD)	XP_016855998.1:n.2128-189_2128-188delinsTA
XM_017000510.1:c.2128-189_2128-188delinsTA (DPYD)	XP_016855999.1:n.2128-189_2128-188delinsTA
NM_000110.4:c.2623-189_2623-188delinsTA (DPYD) MANE Select	NP_000101.2:n.2623-189_2623-188delinsTA