Canonical Allele Identifier: CA425598795

Gene: CAD

Linked Data

• MyVariant Identifiers: chr2:g.27455087T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27232219T>G , CM000664.2:g.27232219T>G	GRCh38
NC_000002.11:g.27455087T>G , CM000664.1:g.27455087T>G	GRCh37
NC_000002.10:g.27308591T>G	NCBI36
NG_046394.1:g.19830T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264705.9:c.2640T>G MANE Select	ENSP00000264705.3:p.Val880=
ENST00000264705.8:c.2640T>G	ENSP00000264705.3:p.Val880=
ENST00000403525.5:c.2451T>G	ENSP00000384510.1:p.Val817=
ENST00000464159.1:n.388T>G
NM_001306079.1:c.2451T>G	NP_001293008.1:p.Val817=
NM_004341.3:c.2640T>G	NP_004332.2:p.Val880=
NM_004341.4:c.2640T>G	NP_004332.2:p.Val880=
XM_005264555.2:c.2640T>G	XP_005264612.1:p.Val880=
XM_005264556.2:c.2640T>G	XP_005264613.1:p.Val880=
XM_005264557.2:c.2640T>G	XP_005264614.1:p.Val880=
XM_006712101.1:c.2451T>G	XP_006712164.1:p.Val817=
XM_006712101.3:c.2451T>G	XP_006712164.1:p.Val817=
XM_024453131.1:c.366T>G	XP_024308899.1:p.Val122=
NM_004341.5:c.2640T>G MANE Select	NP_004332.2:p.Val880=
NM_001306079.2:c.2451T>G	NP_001293008.1:p.Val817=