Canonical Allele Identifier: CA1182878217

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97461379_97461381delinsCTT , CM000663.2:g.97461379_97461381delinsCTT	GRCh38
NC_000001.10:g.97926935_97926937delinsCTT , CM000663.1:g.97926935_97926937delinsCTT	GRCh37
NC_000001.9:g.97699523_97699525delinsCTT	NCBI36
NG_008807.2:g.464679_464681delinsAAG , LRG_722:g.464679_464681delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1741-11158_1741-11156delinsAAG MANE Select	ENSP00000359211.3:n.1741-11158_1741-11156delinsAAG
ENST00000370192.7:c.1741-11158_1741-11156delinsAAG	ENSP00000359211.3:n.1741-11158_1741-11156delinsAAG
NM_000110.3:c.1741-11158_1741-11156delinsAAG , LRG_722t1:c.1741-11158_1741-11156delinsAAG	NP_000101.2:n.1741-11158_1741-11156delinsAAG
XM_005270562.3:c.1525-11158_1525-11156delinsAAG	XP_005270619.2:n.1525-11158_1525-11156delinsAAG
XM_006710397.2:c.1741-11158_1741-11156delinsAAG	XP_006710460.1:n.1741-11158_1741-11156delinsAAG
XM_006710397.3:c.1741-11158_1741-11156delinsAAG	XP_006710460.1:n.1741-11158_1741-11156delinsAAG
XM_017000507.1:c.1630-11158_1630-11156delinsAAG	XP_016855996.1:n.1630-11158_1630-11156delinsAAG
XM_017000508.2:c.1246-11158_1246-11156delinsAAG	XP_016855997.1:n.1246-11158_1246-11156delinsAAG
XM_017000509.2:c.1246-11158_1246-11156delinsAAG	XP_016855998.1:n.1246-11158_1246-11156delinsAAG
XM_017000510.1:c.1246-11158_1246-11156delinsAAG	XP_016855999.1:n.1246-11158_1246-11156delinsAAG
NM_000110.4:c.1741-11158_1741-11156delinsAAG MANE Select	NP_000101.2:n.1741-11158_1741-11156delinsAAG