Canonical Allele Identifier: CA425598783

Gene: CAD

Linked Data

• ClinVar Variation Id: 2779605
• ClinVar RCV Id: RCV003663720
• dbSNP Id: rs1172822796
• gnomAD v3: 2-27232210-C-T
• gnomAD v4: 2-27232210-C-T
• MyVariant Identifiers: chr2:g.27455078C>T (hg19) ; chr2:g.27232210C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232210C>T , CM000664.2:g.27232210C>T	GRCh38
NC_000002.11:g.27455078C>T , CM000664.1:g.27455078C>T	GRCh37
NC_000002.10:g.27308582C>T	NCBI36
NG_046394.1:g.19821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2631C>T MANE Select	ENSP00000264705.3:p.Ala877=
ENST00000264705.8:c.2631C>T	ENSP00000264705.3:p.Ala877=
ENST00000403525.5:c.2442C>T	ENSP00000384510.1:p.Ala814=
ENST00000464159.1:n.379C>T
NM_001306079.1:c.2442C>T	NP_001293008.1:p.Ala814=
NM_004341.3:c.2631C>T	NP_004332.2:p.Ala877=
NM_004341.4:c.2631C>T	NP_004332.2:p.Ala877=
XM_005264555.2:c.2631C>T	XP_005264612.1:p.Ala877=
XM_005264556.2:c.2631C>T	XP_005264613.1:p.Ala877=
XM_005264557.2:c.2631C>T	XP_005264614.1:p.Ala877=
XM_006712101.1:c.2442C>T	XP_006712164.1:p.Ala814=
XM_006712101.3:c.2442C>T	XP_006712164.1:p.Ala814=
XM_024453131.1:c.357C>T	XP_024308899.1:p.Ala119=
NM_004341.5:c.2631C>T MANE Select	NP_004332.2:p.Ala877=
NM_001306079.2:c.2442C>T	NP_001293008.1:p.Ala814=