Canonical Allele Identifier: CA1182843786

Gene: DPYD

Linked Data

• dbSNP Id: rs1672033668

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382517_97382525del , CM000663.2:g.97382517_97382525del	GRCh38
NC_000001.10:g.97848073_97848081del , CM000663.1:g.97848073_97848081del	GRCh37
NC_000001.9:g.97620661_97620669del	NCBI36
NG_008807.2:g.543535_543543del , LRG_722:g.543535_543543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-64_1906-56del MANE Select	ENSP00000359211.3:n.1906-64_1906-56del
ENST00000370192.7:c.1906-64_1906-56del	ENSP00000359211.3:n.1906-64_1906-56del
NM_000110.3:c.1906-64_1906-56del , LRG_722t1:c.1906-64_1906-56del	NP_000101.2:n.1906-64_1906-56del
XM_005270562.3:c.1690-64_1690-56del	XP_005270619.2:n.1690-64_1690-56del
XM_006710397.2:c.1906-64_1906-56del	XP_006710460.1:n.1906-64_1906-56del
XR_947619.1:n.1347-1117_1347-1109del
XR_947620.1:n.1125-1117_1125-1109del
XR_947621.1:n.1347-1117_1347-1109del
XM_006710397.3:c.1906-64_1906-56del	XP_006710460.1:n.1906-64_1906-56del
XM_017000507.1:c.1795-64_1795-56del	XP_016855996.1:n.1795-64_1795-56del
XM_017000508.2:c.1411-64_1411-56del	XP_016855997.1:n.1411-64_1411-56del
XM_017000509.2:c.1411-64_1411-56del	XP_016855998.1:n.1411-64_1411-56del
XM_017000510.1:c.1411-64_1411-56del	XP_016855999.1:n.1411-64_1411-56del
XR_001737686.2:n.692-1117_692-1109del
XR_001737687.1:n.692-1117_692-1109del
XR_001737688.2:n.692-1117_692-1109del
NM_000110.4:c.1906-64_1906-56del MANE Select	NP_000101.2:n.1906-64_1906-56del