Canonical Allele Identifier: CA2646706173

Gene: DPYD

Linked Data

• gnomAD v4: 1-97549416-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549419dup , CM000663.2:g.97549419dup	GRCh38
NC_000001.10:g.98014975dup , CM000663.1:g.98014975dup	GRCh37
NC_000001.9:g.97787563dup	NCBI36
NG_008807.2:g.376643dup , LRG_722:g.376643dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1524+143dup MANE Select	ENSP00000359211.3:n.1524+143dup
ENST00000370192.7:c.1524+143dup	ENSP00000359211.3:n.1524+143dup
NM_000110.3:c.1524+143dup , LRG_722t1:c.1524+143dup	NP_000101.2:n.1524+143dup
XM_005270562.3:c.1524+143dup	XP_005270619.2:n.1524+143dup
XM_006710397.2:c.1524+143dup	XP_006710460.1:n.1524+143dup
XM_006710397.3:c.1524+143dup	XP_006710460.1:n.1524+143dup
XM_017000507.1:c.1413+143dup	XP_016855996.1:n.1413+143dup
XM_017000508.2:c.1029+143dup	XP_016855997.1:n.1029+143dup
XM_017000509.2:c.1029+143dup	XP_016855998.1:n.1029+143dup
XM_017000510.1:c.1029+143dup	XP_016855999.1:n.1029+143dup
NM_000110.4:c.1524+143dup MANE Select	NP_000101.2:n.1524+143dup