Canonical Allele Identifier: CA1573022
Gene: CAD HGNC NCBI

Linked Data

dbSNP Id: rs768180231
gnomAD v2: 2-27454854-G-A
gnomAD v4: 2-27231986-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27231986G>A , CM000664.2:g.27231986G>A GRCh38
NC_000002.11:g.27454854G>A , CM000664.1:g.27454854G>A GRCh37
NC_000002.10:g.27308358G>A NCBI36
NG_046394.1:g.19597G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264705.9:c.2407G>A MANE Select ENSP00000264705.3:p.Glu803Lys
ENST00000264705.8:c.2407G>A ENSP00000264705.3:p.Glu803Lys
ENST00000403525.5:c.2218G>A ENSP00000384510.1:p.Glu740Lys
ENST00000464159.1:n.155G>A
NM_001306079.1:c.2218G>A NP_001293008.1:p.Glu740Lys
NM_004341.3:c.2407G>A NP_004332.2:p.Glu803Lys
NM_004341.4:c.2407G>A NP_004332.2:p.Glu803Lys
XM_005264555.2:c.2407G>A XP_005264612.1:p.Glu803Lys
XM_005264556.2:c.2407G>A XP_005264613.1:p.Glu803Lys
XM_005264557.2:c.2407G>A XP_005264614.1:p.Glu803Lys
XM_006712101.1:c.2218G>A XP_006712164.1:p.Glu740Lys
XM_006712101.3:c.2218G>A XP_006712164.1:p.Glu740Lys
XM_024453131.1:c.133G>A XP_024308899.1:p.Glu45Lys
NM_004341.5:c.2407G>A MANE Select NP_004332.2:p.Glu803Lys
NM_001306079.2:c.2218G>A NP_001293008.1:p.Glu740Lys