Canonical Allele Identifier: CA1240180437

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232430_27232431delinsAC , CM000664.2:g.27232430_27232431delinsAC	GRCh38
NC_000002.11:g.27455298_27455299delinsAC , CM000664.1:g.27455298_27455299delinsAC	GRCh37
NC_000002.10:g.27308802_27308803delinsAC	NCBI36
NG_046394.1:g.20041_20042delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2646-18_2646-17delinsAC MANE Select	ENSP00000264705.3:n.2646-18_2646-17delinsAC
ENST00000264705.8:c.2646-18_2646-17delinsAC	ENSP00000264705.3:n.2646-18_2646-17delinsAC
ENST00000403525.5:c.2457-18_2457-17delinsAC	ENSP00000384510.1:n.2457-18_2457-17delinsAC
ENST00000464159.1:n.394-18_394-17delinsAC
NM_001306079.1:c.2457-18_2457-17delinsAC	NP_001293008.1:n.2457-18_2457-17delinsAC
NM_004341.3:c.2646-18_2646-17delinsAC	NP_004332.2:n.2646-18_2646-17delinsAC
NM_004341.4:c.2646-18_2646-17delinsAC	NP_004332.2:n.2646-18_2646-17delinsAC
XM_005264555.2:c.2646-18_2646-17delinsAC	XP_005264612.1:n.2646-18_2646-17delinsAC
XM_005264556.2:c.2646-18_2646-17delinsAC	XP_005264613.1:n.2646-18_2646-17delinsAC
XM_005264557.2:c.2646-18_2646-17delinsAC	XP_005264614.1:n.2646-18_2646-17delinsAC
XM_006712101.1:c.2457-18_2457-17delinsAC	XP_006712164.1:n.2457-18_2457-17delinsAC
XM_006712101.3:c.2457-18_2457-17delinsAC	XP_006712164.1:n.2457-18_2457-17delinsAC
XM_024453131.1:c.372-18_372-17delinsAC	XP_024308899.1:n.372-18_372-17delinsAC
NM_004341.5:c.2646-18_2646-17delinsAC MANE Select	NP_004332.2:n.2646-18_2646-17delinsAC
NM_001306079.2:c.2457-18_2457-17delinsAC	NP_001293008.1:n.2457-18_2457-17delinsAC