Canonical Allele Identifier: CA1240180220

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27231920_27231921delinsAC , CM000664.2:g.27231920_27231921delinsAC	GRCh38
NC_000002.11:g.27454788_27454789delinsAC , CM000664.1:g.27454788_27454789delinsAC	GRCh37
NC_000002.10:g.27308292_27308293delinsAC	NCBI36
NG_046394.1:g.19531_19532delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2401-60_2401-59delinsAC MANE Select	ENSP00000264705.3:n.2401-60_2401-59delinsAC
ENST00000264705.8:c.2401-60_2401-59delinsAC	ENSP00000264705.3:n.2401-60_2401-59delinsAC
ENST00000403525.5:c.2212-60_2212-59delinsAC	ENSP00000384510.1:n.2212-60_2212-59delinsAC
ENST00000464159.1:n.149-60_149-59delinsAC
NM_001306079.1:c.2212-60_2212-59delinsAC	NP_001293008.1:n.2212-60_2212-59delinsAC
NM_004341.3:c.2401-60_2401-59delinsAC	NP_004332.2:n.2401-60_2401-59delinsAC
NM_004341.4:c.2401-60_2401-59delinsAC	NP_004332.2:n.2401-60_2401-59delinsAC
XM_005264555.2:c.2401-60_2401-59delinsAC	XP_005264612.1:n.2401-60_2401-59delinsAC
XM_005264556.2:c.2401-60_2401-59delinsAC	XP_005264613.1:n.2401-60_2401-59delinsAC
XM_005264557.2:c.2401-60_2401-59delinsAC	XP_005264614.1:n.2401-60_2401-59delinsAC
XM_006712101.1:c.2212-60_2212-59delinsAC	XP_006712164.1:n.2212-60_2212-59delinsAC
XM_006712101.3:c.2212-60_2212-59delinsAC	XP_006712164.1:n.2212-60_2212-59delinsAC
XM_024453131.1:c.127-60_127-59delinsAC	XP_024308899.1:n.127-60_127-59delinsAC
NM_004341.5:c.2401-60_2401-59delinsAC MANE Select	NP_004332.2:n.2401-60_2401-59delinsAC
NM_001306079.2:c.2212-60_2212-59delinsAC	NP_001293008.1:n.2212-60_2212-59delinsAC