Canonical Allele Identifier: CA767356445

Gene: CAD

Linked Data

• dbSNP Id: rs1269302223
• MyVariant Identifiers: chr2:g.27455175_27455176insG (hg19) ; chr2:g.27232307_27232308insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232309dup , CM000664.2:g.27232309dup	GRCh38
NC_000002.11:g.27455177dup , CM000664.1:g.27455177dup	GRCh37
NC_000002.10:g.27308681dup	NCBI36
NG_046394.1:g.19920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2645+85dup MANE Select	ENSP00000264705.3:n.2645+85dup
ENST00000264705.8:c.2645+85dup	ENSP00000264705.3:n.2645+85dup
ENST00000403525.5:c.2456+85dup	ENSP00000384510.1:n.2456+85dup
ENST00000464159.1:n.393+85dup
NM_001306079.1:c.2456+85dup	NP_001293008.1:n.2456+85dup
NM_004341.3:c.2645+85dup	NP_004332.2:n.2645+85dup
NM_004341.4:c.2645+85dup	NP_004332.2:n.2645+85dup
XM_005264555.2:c.2645+85dup	XP_005264612.1:n.2645+85dup
XM_005264556.2:c.2645+85dup	XP_005264613.1:n.2645+85dup
XM_005264557.2:c.2645+85dup	XP_005264614.1:n.2645+85dup
XM_006712101.1:c.2456+85dup	XP_006712164.1:n.2456+85dup
XM_006712101.3:c.2456+85dup	XP_006712164.1:n.2456+85dup
XM_024453131.1:c.371+85dup	XP_024308899.1:n.371+85dup
NM_004341.5:c.2645+85dup MANE Select	NP_004332.2:n.2645+85dup
NM_001306079.2:c.2456+85dup	NP_001293008.1:n.2456+85dup