Canonical Allele Identifier: CA346211968

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27455050G>T (hg19) ; chr2:g.27232182G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232182G>T , CM000664.2:g.27232182G>T	GRCh38
NC_000002.11:g.27455050G>T , CM000664.1:g.27455050G>T	GRCh37
NC_000002.10:g.27308554G>T	NCBI36
NG_046394.1:g.19793G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2603G>T MANE Select	ENSP00000264705.3:p.Cys868Phe
ENST00000264705.8:c.2603G>T	ENSP00000264705.3:p.Cys868Phe
ENST00000403525.5:c.2414G>T	ENSP00000384510.1:p.Cys805Phe
ENST00000464159.1:n.351G>T
NM_001306079.1:c.2414G>T	NP_001293008.1:p.Cys805Phe
NM_004341.3:c.2603G>T	NP_004332.2:p.Cys868Phe
NM_004341.4:c.2603G>T	NP_004332.2:p.Cys868Phe
XM_005264555.2:c.2603G>T	XP_005264612.1:p.Cys868Phe
XM_005264556.2:c.2603G>T	XP_005264613.1:p.Cys868Phe
XM_005264557.2:c.2603G>T	XP_005264614.1:p.Cys868Phe
XM_006712101.1:c.2414G>T	XP_006712164.1:p.Cys805Phe
XM_006712101.3:c.2414G>T	XP_006712164.1:p.Cys805Phe
XM_024453131.1:c.329G>T	XP_024308899.1:p.Cys110Phe
NM_004341.5:c.2603G>T MANE Select	NP_004332.2:p.Cys868Phe
NM_001306079.2:c.2414G>T	NP_001293008.1:p.Cys805Phe