Canonical Allele Identifier: CA767356436

Gene: CAD

Linked Data

• dbSNP Id: rs1260451303
• MyVariant Identifiers: chr2:g.27454846del (hg19) ; chr2:g.27231978del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27231978del , CM000664.2:g.27231978del	GRCh38
NC_000002.11:g.27454846del , CM000664.1:g.27454846del	GRCh37
NC_000002.10:g.27308350del	NCBI36
NG_046394.1:g.19589del

Transcript Alleles

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