Canonical Allele Identifier: CA1240180216
Gene: CAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27231905_27231907delinsCAA , CM000664.2:g.27231905_27231907delinsCAA GRCh38
NC_000002.11:g.27454773_27454775delinsCAA , CM000664.1:g.27454773_27454775delinsCAA GRCh37
NC_000002.10:g.27308277_27308279delinsCAA NCBI36
NG_046394.1:g.19516_19518delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264705.9:c.2401-75_2401-73delinsCAA MANE Select ENSP00000264705.3:n.2401-75_2401-73delinsCAA
ENST00000264705.8:c.2401-75_2401-73delinsCAA ENSP00000264705.3:n.2401-75_2401-73delinsCAA
ENST00000403525.5:c.2212-75_2212-73delinsCAA ENSP00000384510.1:n.2212-75_2212-73delinsCAA
ENST00000464159.1:n.149-75_149-73delinsCAA
NM_001306079.1:c.2212-75_2212-73delinsCAA NP_001293008.1:n.2212-75_2212-73delinsCAA
NM_004341.3:c.2401-75_2401-73delinsCAA NP_004332.2:n.2401-75_2401-73delinsCAA
NM_004341.4:c.2401-75_2401-73delinsCAA NP_004332.2:n.2401-75_2401-73delinsCAA
XM_005264555.2:c.2401-75_2401-73delinsCAA XP_005264612.1:n.2401-75_2401-73delinsCAA
XM_005264556.2:c.2401-75_2401-73delinsCAA XP_005264613.1:n.2401-75_2401-73delinsCAA
XM_005264557.2:c.2401-75_2401-73delinsCAA XP_005264614.1:n.2401-75_2401-73delinsCAA
XM_006712101.1:c.2212-75_2212-73delinsCAA XP_006712164.1:n.2212-75_2212-73delinsCAA
XM_006712101.3:c.2212-75_2212-73delinsCAA XP_006712164.1:n.2212-75_2212-73delinsCAA
XM_024453131.1:c.127-75_127-73delinsCAA XP_024308899.1:n.127-75_127-73delinsCAA
NM_004341.5:c.2401-75_2401-73delinsCAA MANE Select NP_004332.2:n.2401-75_2401-73delinsCAA
NM_001306079.2:c.2212-75_2212-73delinsCAA NP_001293008.1:n.2212-75_2212-73delinsCAA