Canonical Allele Identifier: CA346212131

Gene: CAD

Linked Data

• gnomAD v4: 2-27232214-G-A
• MyVariant Identifiers: chr2:g.27455082G>A (hg19) ; chr2:g.27232214G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232214G>A , CM000664.2:g.27232214G>A	GRCh38
NC_000002.11:g.27455082G>A , CM000664.1:g.27455082G>A	GRCh37
NC_000002.10:g.27308586G>A	NCBI36
NG_046394.1:g.19825G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2635G>A MANE Select	ENSP00000264705.3:p.Ala879Thr
ENST00000264705.8:c.2635G>A	ENSP00000264705.3:p.Ala879Thr
ENST00000403525.5:c.2446G>A	ENSP00000384510.1:p.Ala816Thr
ENST00000464159.1:n.383G>A
NM_001306079.1:c.2446G>A	NP_001293008.1:p.Ala816Thr
NM_004341.3:c.2635G>A	NP_004332.2:p.Ala879Thr
NM_004341.4:c.2635G>A	NP_004332.2:p.Ala879Thr
XM_005264555.2:c.2635G>A	XP_005264612.1:p.Ala879Thr
XM_005264556.2:c.2635G>A	XP_005264613.1:p.Ala879Thr
XM_005264557.2:c.2635G>A	XP_005264614.1:p.Ala879Thr
XM_006712101.1:c.2446G>A	XP_006712164.1:p.Ala816Thr
XM_006712101.3:c.2446G>A	XP_006712164.1:p.Ala816Thr
XM_024453131.1:c.361G>A	XP_024308899.1:p.Ala121Thr
NM_004341.5:c.2635G>A MANE Select	NP_004332.2:p.Ala879Thr
NM_001306079.2:c.2446G>A	NP_001293008.1:p.Ala816Thr