Canonical Allele Identifier: CA1182843791

Gene: DPYD

Linked Data

• dbSNP Id: rs1672034267

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382525_97382527dup , CM000663.2:g.97382525_97382527dup	GRCh38
NC_000001.10:g.97848081_97848083dup , CM000663.1:g.97848081_97848083dup	GRCh37
NC_000001.9:g.97620669_97620671dup	NCBI36
NG_008807.2:g.543535_543537dup , LRG_722:g.543535_543537dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-64_1906-62dup MANE Select	ENSP00000359211.3:n.1906-64_1906-62dup
ENST00000370192.7:c.1906-64_1906-62dup	ENSP00000359211.3:n.1906-64_1906-62dup
NM_000110.3:c.1906-64_1906-62dup , LRG_722t1:c.1906-64_1906-62dup	NP_000101.2:n.1906-64_1906-62dup
XM_005270562.3:c.1690-64_1690-62dup	XP_005270619.2:n.1690-64_1690-62dup
XM_006710397.2:c.1906-64_1906-62dup	XP_006710460.1:n.1906-64_1906-62dup
XR_947619.1:n.1347-1109_1347-1107dup
XR_947620.1:n.1125-1109_1125-1107dup
XR_947621.1:n.1347-1109_1347-1107dup
XM_006710397.3:c.1906-64_1906-62dup	XP_006710460.1:n.1906-64_1906-62dup
XM_017000507.1:c.1795-64_1795-62dup	XP_016855996.1:n.1795-64_1795-62dup
XM_017000508.2:c.1411-64_1411-62dup	XP_016855997.1:n.1411-64_1411-62dup
XM_017000509.2:c.1411-64_1411-62dup	XP_016855998.1:n.1411-64_1411-62dup
XM_017000510.1:c.1411-64_1411-62dup	XP_016855999.1:n.1411-64_1411-62dup
XR_001737686.2:n.692-1109_692-1107dup
XR_001737687.1:n.692-1109_692-1107dup
XR_001737688.2:n.692-1109_692-1107dup
NM_000110.4:c.1906-64_1906-62dup MANE Select	NP_000101.2:n.1906-64_1906-62dup