Canonical Allele Identifier: CA2646705505

Gene: DPYD

Linked Data

• gnomAD v4: 1-97449914-ATCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97449918_97449921del , CM000663.2:g.97449918_97449921del	GRCh38
NC_000001.10:g.97915474_97915477del , CM000663.1:g.97915474_97915477del	GRCh37
NC_000001.9:g.97688062_97688065del	NCBI36
NG_008807.2:g.476142_476145del , LRG_722:g.476142_476145del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+141_1905+144del MANE Select	ENSP00000359211.3:n.1905+141_1905+144del
ENST00000370192.7:c.1905+141_1905+144del	ENSP00000359211.3:n.1905+141_1905+144del
NM_000110.3:c.1905+141_1905+144del , LRG_722t1:c.1905+141_1905+144del	NP_000101.2:n.1905+141_1905+144del
XM_005270562.3:c.1689+141_1689+144del	XP_005270619.2:n.1689+141_1689+144del
XM_006710397.2:c.1905+141_1905+144del	XP_006710460.1:n.1905+141_1905+144del
XM_006710397.3:c.1905+141_1905+144del	XP_006710460.1:n.1905+141_1905+144del
XM_017000507.1:c.1794+141_1794+144del	XP_016855996.1:n.1794+141_1794+144del
XM_017000508.2:c.1410+141_1410+144del	XP_016855997.1:n.1410+141_1410+144del
XM_017000509.2:c.1410+141_1410+144del	XP_016855998.1:n.1410+141_1410+144del
XM_017000510.1:c.1410+141_1410+144del	XP_016855999.1:n.1410+141_1410+144del
NM_000110.4:c.1905+141_1905+144del MANE Select	NP_000101.2:n.1905+141_1905+144del