Canonical Allele Identifier: CA2646705574

Gene: DPYD

Linked Data

• gnomAD v4: 1-97450049-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450053_97450054del , CM000663.2:g.97450053_97450054del	GRCh38
NC_000001.10:g.97915609_97915610del , CM000663.1:g.97915609_97915610del	GRCh37
NC_000001.9:g.97688197_97688198del	NCBI36
NG_008807.2:g.476009_476010del , LRG_722:g.476009_476010del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+8_1905+9del MANE Select	ENSP00000359211.3:n.1905+8_1905+9del
ENST00000370192.7:c.1905+8_1905+9del	ENSP00000359211.3:n.1905+8_1905+9del
NM_000110.3:c.1905+8_1905+9del , LRG_722t1:c.1905+8_1905+9del	NP_000101.2:n.1905+8_1905+9del
XM_005270562.3:c.1689+8_1689+9del	XP_005270619.2:n.1689+8_1689+9del
XM_006710397.2:c.1905+8_1905+9del	XP_006710460.1:n.1905+8_1905+9del
XM_006710397.3:c.1905+8_1905+9del	XP_006710460.1:n.1905+8_1905+9del
XM_017000507.1:c.1794+8_1794+9del	XP_016855996.1:n.1794+8_1794+9del
XM_017000508.2:c.1410+8_1410+9del	XP_016855997.1:n.1410+8_1410+9del
XM_017000509.2:c.1410+8_1410+9del	XP_016855998.1:n.1410+8_1410+9del
XM_017000510.1:c.1410+8_1410+9del	XP_016855999.1:n.1410+8_1410+9del
NM_000110.4:c.1905+8_1905+9del MANE Select	NP_000101.2:n.1905+8_1905+9del