Canonical Allele Identifier: CA1240180293

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232104G= , CM000664.2:g.27232104G=	GRCh38
NC_000002.11:g.27454972G= , CM000664.1:g.27454972G=	GRCh37
NC_000002.10:g.27308476G=	NCBI36
NG_046394.1:g.19715G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264705.9:c.2525G= MANE Select	ENSP00000264705.3:p.Arg842=
ENST00000264705.8:c.2525G=	ENSP00000264705.3:p.Arg842=
ENST00000403525.5:c.2336G=	ENSP00000384510.1:p.Arg779=
ENST00000464159.1:n.273G=
NM_001306079.1:c.2336G=	NP_001293008.1:p.Arg779=
NM_004341.3:c.2525G=	NP_004332.2:p.Arg842=
NM_004341.4:c.2525G=	NP_004332.2:p.Arg842=
XM_005264555.2:c.2525G=	XP_005264612.1:p.Arg842=
XM_005264556.2:c.2525G=	XP_005264613.1:p.Arg842=
XM_005264557.2:c.2525G=	XP_005264614.1:p.Arg842=
XM_006712101.1:c.2336G=	XP_006712164.1:p.Arg779=
XM_006712101.3:c.2336G=	XP_006712164.1:p.Arg779=
XM_024453131.1:c.251G=	XP_024308899.1:p.Arg84=
NM_004341.5:c.2525G= MANE Select	NP_004332.2:p.Arg842=
NM_001306079.2:c.2336G=	NP_001293008.1:p.Arg779=