Canonical Allele Identifier: CA425598707

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27455024G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232156G>C , CM000664.2:g.27232156G>C	GRCh38
NC_000002.11:g.27455024G>C , CM000664.1:g.27455024G>C	GRCh37
NC_000002.10:g.27308528G>C	NCBI36
NG_046394.1:g.19767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2577G>C MANE Select	ENSP00000264705.3:p.Pro859=
ENST00000264705.8:c.2577G>C	ENSP00000264705.3:p.Pro859=
ENST00000403525.5:c.2388G>C	ENSP00000384510.1:p.Pro796=
ENST00000464159.1:n.325G>C
NM_001306079.1:c.2388G>C	NP_001293008.1:p.Pro796=
NM_004341.3:c.2577G>C	NP_004332.2:p.Pro859=
NM_004341.4:c.2577G>C	NP_004332.2:p.Pro859=
XM_005264555.2:c.2577G>C	XP_005264612.1:p.Pro859=
XM_005264556.2:c.2577G>C	XP_005264613.1:p.Pro859=
XM_005264557.2:c.2577G>C	XP_005264614.1:p.Pro859=
XM_006712101.1:c.2388G>C	XP_006712164.1:p.Pro796=
XM_006712101.3:c.2388G>C	XP_006712164.1:p.Pro796=
XM_024453131.1:c.303G>C	XP_024308899.1:p.Pro101=
NM_004341.5:c.2577G>C MANE Select	NP_004332.2:p.Pro859=
NM_001306079.2:c.2388G>C	NP_001293008.1:p.Pro796=