Canonical Allele Identifier: CA2646706354

Gene: DPYD

Linked Data

• gnomAD v4: 1-97573700-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97573702_97573703del , CM000663.2:g.97573702_97573703del	GRCh38
NC_000001.10:g.98039258_98039259del , CM000663.1:g.98039258_98039259del	GRCh37
NC_000001.9:g.97811846_97811847del	NCBI36
NG_008807.2:g.352358_352359del , LRG_722:g.352358_352359del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1339+58_1339+59del MANE Select	ENSP00000359211.3:n.1339+58_1339+59del
ENST00000370192.7:c.1339+58_1339+59del	ENSP00000359211.3:n.1339+58_1339+59del
NM_000110.3:c.1339+58_1339+59del , LRG_722t1:c.1339+58_1339+59del	NP_000101.2:n.1339+58_1339+59del
XM_005270562.3:c.1339+58_1339+59del	XP_005270619.2:n.1339+58_1339+59del
XM_006710397.2:c.1339+58_1339+59del	XP_006710460.1:n.1339+58_1339+59del
XM_006710397.3:c.1339+58_1339+59del	XP_006710460.1:n.1339+58_1339+59del
XM_017000507.1:c.1228+58_1228+59del	XP_016855996.1:n.1228+58_1228+59del
XM_017000508.2:c.844+58_844+59del	XP_016855997.1:n.844+58_844+59del
XM_017000509.2:c.844+58_844+59del	XP_016855998.1:n.844+58_844+59del
XM_017000510.1:c.844+58_844+59del	XP_016855999.1:n.844+58_844+59del
NM_000110.4:c.1339+58_1339+59del MANE Select	NP_000101.2:n.1339+58_1339+59del