Canonical Allele Identifier: CA1240180146

Gene: CAD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27231766T= , CM000664.2:g.27231766T=	GRCh38
NC_000002.11:g.27454634T= , CM000664.1:g.27454634T=	GRCh37
NC_000002.10:g.27308138T=	NCBI36
NG_046394.1:g.19377T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2400+186T= MANE Select	ENSP00000264705.3:n.2400+186T=
ENST00000264705.8:c.2400+186T=	ENSP00000264705.3:n.2400+186T=
ENST00000403525.5:c.2211+186T=	ENSP00000384510.1:n.2211+186T=
ENST00000464159.1:n.148+186T=
NM_001306079.1:c.2211+186T=	NP_001293008.1:n.2211+186T=
NM_004341.3:c.2400+186T=	NP_004332.2:n.2400+186T=
NM_004341.4:c.2400+186T=	NP_004332.2:n.2400+186T=
XM_005264555.2:c.2400+186T=	XP_005264612.1:n.2400+186T=
XM_005264556.2:c.2400+186T=	XP_005264613.1:n.2400+186T=
XM_005264557.2:c.2400+186T=	XP_005264614.1:n.2400+186T=
XM_006712101.1:c.2211+186T=	XP_006712164.1:n.2211+186T=
XM_006712101.3:c.2211+186T=	XP_006712164.1:n.2211+186T=
XM_024453131.1:c.126+186T=	XP_024308899.1:n.126+186T=
NM_004341.5:c.2400+186T= MANE Select	NP_004332.2:n.2400+186T=
NM_001306079.2:c.2211+186T=	NP_001293008.1:n.2211+186T=