Canonical Allele Identifier: CA1182843849

Gene: DPYD

Linked Data

• dbSNP Id: rs1672043939

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382670dup , CM000663.2:g.97382670dup	GRCh38
NC_000001.10:g.97848226dup , CM000663.1:g.97848226dup	GRCh37
NC_000001.9:g.97620814dup	NCBI36
NG_008807.2:g.543393dup , LRG_722:g.543393dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-206dup MANE Select	ENSP00000359211.3:n.1906-206dup
ENST00000370192.7:c.1906-206dup	ENSP00000359211.3:n.1906-206dup
NM_000110.3:c.1906-206dup , LRG_722t1:c.1906-206dup	NP_000101.2:n.1906-206dup
XM_005270562.3:c.1690-206dup	XP_005270619.2:n.1690-206dup
XM_006710397.2:c.1906-206dup	XP_006710460.1:n.1906-206dup
XR_947619.1:n.1347-964dup
XR_947620.1:n.1125-964dup
XR_947621.1:n.1347-964dup
XM_006710397.3:c.1906-206dup	XP_006710460.1:n.1906-206dup
XM_017000507.1:c.1795-206dup	XP_016855996.1:n.1795-206dup
XM_017000508.2:c.1411-206dup	XP_016855997.1:n.1411-206dup
XM_017000509.2:c.1411-206dup	XP_016855998.1:n.1411-206dup
XM_017000510.1:c.1411-206dup	XP_016855999.1:n.1411-206dup
XR_001737686.2:n.692-964dup
XR_001737687.1:n.692-964dup
XR_001737688.2:n.692-964dup
NM_000110.4:c.1906-206dup MANE Select	NP_000101.2:n.1906-206dup