Canonical Allele Identifier: CA346211169

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27454860C>A (hg19) ; chr2:g.27231992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27231992C>A , CM000664.2:g.27231992C>A	GRCh38
NC_000002.11:g.27454860C>A , CM000664.1:g.27454860C>A	GRCh37
NC_000002.10:g.27308364C>A	NCBI36
NG_046394.1:g.19603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2413C>A MANE Select	ENSP00000264705.3:p.Pro805Thr
ENST00000264705.8:c.2413C>A	ENSP00000264705.3:p.Pro805Thr
ENST00000403525.5:c.2224C>A	ENSP00000384510.1:p.Pro742Thr
ENST00000464159.1:n.161C>A
NM_001306079.1:c.2224C>A	NP_001293008.1:p.Pro742Thr
NM_004341.3:c.2413C>A	NP_004332.2:p.Pro805Thr
NM_004341.4:c.2413C>A	NP_004332.2:p.Pro805Thr
XM_005264555.2:c.2413C>A	XP_005264612.1:p.Pro805Thr
XM_005264556.2:c.2413C>A	XP_005264613.1:p.Pro805Thr
XM_005264557.2:c.2413C>A	XP_005264614.1:p.Pro805Thr
XM_006712101.1:c.2224C>A	XP_006712164.1:p.Pro742Thr
XM_006712101.3:c.2224C>A	XP_006712164.1:p.Pro742Thr
XM_024453131.1:c.139C>A	XP_024308899.1:p.Pro47Thr
NM_004341.5:c.2413C>A MANE Select	NP_004332.2:p.Pro805Thr
NM_001306079.2:c.2224C>A	NP_001293008.1:p.Pro742Thr