Canonical Allele Identifier: CA2646703417

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97098711-TATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098713_97098715del , CM000663.2:g.97098713_97098715del	GRCh38
NC_000001.10:g.97564269_97564271del , CM000663.1:g.97564269_97564271del	GRCh37
NC_000001.9:g.97336857_97336859del	NCBI36
NG_008807.2:g.827346_827348del , LRG_722:g.827346_827348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-82_2623-80del (DPYD) MANE Select	ENSP00000359211.3:n.2623-82_2623-80del
ENST00000370192.7:c.2623-82_2623-80del (DPYD)	ENSP00000359211.3:n.2623-82_2623-80del
NM_000110.3:c.2623-82_2623-80del , LRG_722t1:c.2623-82_2623-80del (DPYD)	NP_000101.2:n.2623-82_2623-80del
NR_046590.1:n.64+2727_64+2729del (DPYD-AS1)
XM_005270562.3:c.2407-82_2407-80del (DPYD)	XP_005270619.2:n.2407-82_2407-80del
XM_017000507.1:c.2512-82_2512-80del (DPYD)	XP_016855996.1:n.2512-82_2512-80del
XM_017000508.2:c.2128-82_2128-80del (DPYD)	XP_016855997.1:n.2128-82_2128-80del
XM_017000509.2:c.2128-82_2128-80del (DPYD)	XP_016855998.1:n.2128-82_2128-80del
XM_017000510.1:c.2128-82_2128-80del (DPYD)	XP_016855999.1:n.2128-82_2128-80del
NM_000110.4:c.2623-82_2623-80del (DPYD) MANE Select	NP_000101.2:n.2623-82_2623-80del