Canonical Allele Identifier: CA425384861

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27454964A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232096A>C , CM000664.2:g.27232096A>C	GRCh38
NC_000002.11:g.27454964A>C , CM000664.1:g.27454964A>C	GRCh37
NC_000002.10:g.27308468A>C	NCBI36
NG_046394.1:g.19707A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264705.9:c.2517A>C MANE Select	ENSP00000264705.3:p.Arg839=
ENST00000264705.8:c.2517A>C	ENSP00000264705.3:p.Arg839=
ENST00000403525.5:c.2328A>C	ENSP00000384510.1:p.Arg776=
ENST00000464159.1:n.265A>C
NM_001306079.1:c.2328A>C	NP_001293008.1:p.Arg776=
NM_004341.3:c.2517A>C	NP_004332.2:p.Arg839=
NM_004341.4:c.2517A>C	NP_004332.2:p.Arg839=
XM_005264555.2:c.2517A>C	XP_005264612.1:p.Arg839=
XM_005264556.2:c.2517A>C	XP_005264613.1:p.Arg839=
XM_005264557.2:c.2517A>C	XP_005264614.1:p.Arg839=
XM_006712101.1:c.2328A>C	XP_006712164.1:p.Arg776=
XM_006712101.3:c.2328A>C	XP_006712164.1:p.Arg776=
XM_024453131.1:c.243A>C	XP_024308899.1:p.Arg81=
NM_004341.5:c.2517A>C MANE Select	NP_004332.2:p.Arg839=
NM_001306079.2:c.2328A>C	NP_001293008.1:p.Arg776=