Canonical Allele Identifier: CA2658308876

Gene: CAD

Linked Data

• gnomAD v4: 2-27232341-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232341C>A , CM000664.2:g.27232341C>A	GRCh38
NC_000002.11:g.27455209C>A , CM000664.1:g.27455209C>A	GRCh37
NC_000002.10:g.27308713C>A	NCBI36
NG_046394.1:g.19952C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2646-107C>A MANE Select	ENSP00000264705.3:n.2646-107C>A
ENST00000264705.8:c.2646-107C>A	ENSP00000264705.3:n.2646-107C>A
ENST00000403525.5:c.2457-107C>A	ENSP00000384510.1:n.2457-107C>A
ENST00000464159.1:n.394-107C>A
NM_001306079.1:c.2457-107C>A	NP_001293008.1:n.2457-107C>A
NM_004341.3:c.2646-107C>A	NP_004332.2:n.2646-107C>A
NM_004341.4:c.2646-107C>A	NP_004332.2:n.2646-107C>A
XM_005264555.2:c.2646-107C>A	XP_005264612.1:n.2646-107C>A
XM_005264556.2:c.2646-107C>A	XP_005264613.1:n.2646-107C>A
XM_005264557.2:c.2646-107C>A	XP_005264614.1:n.2646-107C>A
XM_006712101.1:c.2457-107C>A	XP_006712164.1:n.2457-107C>A
XM_006712101.3:c.2457-107C>A	XP_006712164.1:n.2457-107C>A
XM_024453131.1:c.372-107C>A	XP_024308899.1:n.372-107C>A
NM_004341.5:c.2646-107C>A MANE Select	NP_004332.2:n.2646-107C>A
NM_001306079.2:c.2457-107C>A	NP_001293008.1:n.2457-107C>A