Canonical Allele Identifier: CA2646705565

Gene: DPYD

Linked Data

• gnomAD v4: 1-97450017-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450018_97450019del , CM000663.2:g.97450018_97450019del	GRCh38
NC_000001.10:g.97915574_97915575del , CM000663.1:g.97915574_97915575del	GRCh37
NC_000001.9:g.97688162_97688163del	NCBI36
NG_008807.2:g.476041_476042del , LRG_722:g.476041_476042del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+40_1905+41del MANE Select	ENSP00000359211.3:n.1905+40_1905+41del
ENST00000370192.7:c.1905+40_1905+41del	ENSP00000359211.3:n.1905+40_1905+41del
NM_000110.3:c.1905+40_1905+41del , LRG_722t1:c.1905+40_1905+41del	NP_000101.2:n.1905+40_1905+41del
XM_005270562.3:c.1689+40_1689+41del	XP_005270619.2:n.1689+40_1689+41del
XM_006710397.2:c.1905+40_1905+41del	XP_006710460.1:n.1905+40_1905+41del
XM_006710397.3:c.1905+40_1905+41del	XP_006710460.1:n.1905+40_1905+41del
XM_017000507.1:c.1794+40_1794+41del	XP_016855996.1:n.1794+40_1794+41del
XM_017000508.2:c.1410+40_1410+41del	XP_016855997.1:n.1410+40_1410+41del
XM_017000509.2:c.1410+40_1410+41del	XP_016855998.1:n.1410+40_1410+41del
XM_017000510.1:c.1410+40_1410+41del	XP_016855999.1:n.1410+40_1410+41del
NM_000110.4:c.1905+40_1905+41del MANE Select	NP_000101.2:n.1905+40_1905+41del