Canonical Allele Identifier: CA2558027213

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549657_97549658insTGCCCGGCCTCTCTGGTCTCGAAACCCTCTCCGCCATCAAAGACTTGCATCCTGAGATG , CM000663.2:g.97549657_97549658insTGCCCGGCCTCTCTGGTCTCGAAACCCTCTCCGCCATCAAAGACTTGCATCCTGAGATG	GRCh38
NC_000001.10:g.98015213_98015214insTGCCCGGCCTCTCTGGTCTCGAAACCCTCTCCGCCATCAAAGACTTGCATCCTGAGATG , CM000663.1:g.98015213_98015214insTGCCCGGCCTCTCTGGTCTCGAAACCCTCTCCGCCATCAAAGACTTGCATCCTGAGATG	GRCh37
NC_000001.9:g.97787801_97787802insTGCCCGGCCTCTCTGGTCTCGAAACCCTCTCCGCCATCAAAGACTTGCATCCTGAGATG	NCBI36
NG_008807.2:g.376402_376403insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA , LRG_722:g.376402_376403insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA MANE Select	ENSP00000359211.3:p.Val476AlafsTer8
ENST00000370192.7:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	ENSP00000359211.3:p.Val476AlafsTer8
NM_000110.3:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA , LRG_722t1:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	NP_000101.2:p.Val476AlafsTer8
XM_005270562.3:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_005270619.2:p.Val476AlafsTer8
XM_006710397.2:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_006710460.1:p.Val476AlafsTer8
XM_006710397.3:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_006710460.1:p.Val476AlafsTer8
XM_017000507.1:c.1315_1316insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_016855996.1:p.Val439AlafsTer8
XM_017000508.2:c.931_932insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_016855997.1:p.Val311AlafsTer8
XM_017000509.2:c.931_932insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_016855998.1:p.Val311AlafsTer8
XM_017000510.1:c.931_932insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA	XP_016855999.1:p.Val311AlafsTer8
NM_000110.4:c.1426_1427insCATCTCAGGATGCAAGTCTTTGATGGCGGAGAGGGTTTCGAGACCAGAGAGGCCGGGCA MANE Select	NP_000101.2:p.Val476AlafsTer8