Canonical Allele Identifier: CA1240180311

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232155C= , CM000664.2:g.27232155C=	GRCh38
NC_000002.11:g.27455023C= , CM000664.1:g.27455023C=	GRCh37
NC_000002.10:g.27308527C=	NCBI36
NG_046394.1:g.19766C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2576C= MANE Select	ENSP00000264705.3:p.Pro859=
ENST00000264705.8:c.2576C=	ENSP00000264705.3:p.Pro859=
ENST00000403525.5:c.2387C=	ENSP00000384510.1:p.Pro796=
ENST00000464159.1:n.324C=
NM_001306079.1:c.2387C=	NP_001293008.1:p.Pro796=
NM_004341.3:c.2576C=	NP_004332.2:p.Pro859=
NM_004341.4:c.2576C=	NP_004332.2:p.Pro859=
XM_005264555.2:c.2576C=	XP_005264612.1:p.Pro859=
XM_005264556.2:c.2576C=	XP_005264613.1:p.Pro859=
XM_005264557.2:c.2576C=	XP_005264614.1:p.Pro859=
XM_006712101.1:c.2387C=	XP_006712164.1:p.Pro796=
XM_006712101.3:c.2387C=	XP_006712164.1:p.Pro796=
XM_024453131.1:c.302C=	XP_024308899.1:p.Pro101=
NM_004341.5:c.2576C= MANE Select	NP_004332.2:p.Pro859=
NM_001306079.2:c.2387C=	NP_001293008.1:p.Pro796=