Canonical Allele Identifier: CA1004794445

Gene: DPYD

Linked Data

• dbSNP Id: rs1661007089
• gnomAD v3: 1-97691523-C-CT
• gnomAD v4: 1-97691523-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691523_97691524insT , CM000663.2:g.97691523_97691524insT	GRCh38
NC_000001.10:g.98157079_98157080insT , CM000663.1:g.98157079_98157080insT	GRCh37
NC_000001.9:g.97929667_97929668insT	NCBI36
NG_008807.2:g.234536_234537insA , LRG_722:g.234536_234537insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+193_762+194insA MANE Select	ENSP00000359211.3:n.762+193_762+194insA
ENST00000370192.7:c.762+193_762+194insA	ENSP00000359211.3:n.762+193_762+194insA
ENST00000474241.1:n.719_720insA
NM_000110.3:c.762+193_762+194insA , LRG_722t1:c.762+193_762+194insA	NP_000101.2:n.762+193_762+194insA
XM_005270562.3:c.762+193_762+194insA	XP_005270619.2:n.762+193_762+194insA
XM_006710397.2:c.762+193_762+194insA	XP_006710460.1:n.762+193_762+194insA
XM_006710397.3:c.762+193_762+194insA	XP_006710460.1:n.762+193_762+194insA
XM_017000507.1:c.651+193_651+194insA	XP_016855996.1:n.651+193_651+194insA
XM_017000508.2:c.267+193_267+194insA	XP_016855997.1:n.267+193_267+194insA
XM_017000509.2:c.267+193_267+194insA	XP_016855998.1:n.267+193_267+194insA
XM_017000510.1:c.267+193_267+194insA	XP_016855999.1:n.267+193_267+194insA
NM_000110.4:c.762+193_762+194insA MANE Select	NP_000101.2:n.762+193_762+194insA