Canonical Allele Identifier: CA531763960

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27237527_27237532del , CM000664.2:g.27237527_27237532del	GRCh38
NC_000002.11:g.27460395_27460400del , CM000664.1:g.27460395_27460400del	GRCh37
NC_000002.10:g.27313899_27313904del	NCBI36
NG_046394.1:g.25138_25143del

Transcript Alleles

HGVS	Amino-acid Change
NM_004341.5:c.4545_4550del MANE Select	NP_004332.2:p.Leu1516_Ala1517del
ENST00000264705.9:c.4545_4550del MANE Select	ENSP00000264705.3:p.Leu1516_Ala1517del
NM_001306079.1:c.4356_4361del	NP_001293008.1:p.Leu1453_Ala1454del
NM_001306079.2:c.4356_4361del	NP_001293008.1:p.Leu1453_Ala1454del
NM_004341.3:c.4545_4550del	NP_004332.2:p.Leu1516_Ala1517del
NM_004341.4:c.4545_4550del	NP_004332.2:p.Leu1516_Ala1517del
ENST00000264705.8:c.4545_4550del	ENSP00000264705.3:p.Leu1516_Ala1517del
ENST00000403525.5:c.4356_4361del	ENSP00000384510.1:p.Leu1453_Ala1454del
ENST00000458503.1:c.500_505del
XM_005264555.2:c.4545_4550del	XP_005264612.1:p.Leu1516_Ala1517del
XM_005264556.2:c.4545_4550del	XP_005264613.1:p.Leu1516_Ala1517del
XM_005264557.2:c.4545_4550del	XP_005264614.1:p.Leu1516_Ala1517del
XM_006712101.1:c.4356_4361del	XP_006712164.1:p.Leu1453_Ala1454del
XM_006712101.3:c.4356_4361del	XP_006712164.1:p.Leu1453_Ala1454del
XM_024453131.1:c.2271_2276del	XP_024308899.1:p.Leu758_Ala759del