Canonical Allele Identifier: CA454888630

Gene: CCM2

Linked Data

• MyVariant Identifiers: chr7:g.45108166T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068567T>A , CM000669.2:g.45068567T>A	GRCh38
NC_000007.13:g.45108166T>A , CM000669.1:g.45108166T>A	GRCh37
NC_000007.12:g.45074691T>A	NCBI36
NG_016295.1:g.73380T>A , LRG_664:g.73380T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.597T>A MANE Select	ENSP00000258781.7:p.Ala199=
ENST00000648329.1:c.597T>A	ENSP00000496916.1:p.Ala199=
ENST00000258781.10:c.597T>A	ENSP00000258781.6:p.Ala199=
ENST00000381112.7:c.660T>A	ENSP00000370503.3:p.Ala220=
ENST00000461377.5:n.950T>A
ENST00000472223.5:n.664T>A
ENST00000474617.1:c.454+3921T>A	ENSP00000419474.1:n.454+3921T>A
ENST00000475551.5:c.579T>A	ENSP00000417180.1:p.Ala193=
ENST00000477605.1:n.932T>A
ENST00000478582.5:n.684-1259T>A
ENST00000480382.1:c.74T>A
ENST00000480658.5:n.425T>A
ENST00000481194.1:n.45-1259T>A
ENST00000482714.5:n.519T>A
ENST00000488727.5:c.597T>A	ENSP00000417251.1:p.Ala199=
ENST00000492883.5:n.485-1259T>A
ENST00000541586.5:c.423T>A	ENSP00000444725.1:p.Ala141=
ENST00000544363.5:c.472+3921T>A	ENSP00000438035.1:n.472+3921T>A
NM_001029835.2:c.660T>A , LRG_664t1:c.660T>A	NP_001025006.1:p.Ala220=
NM_001167934.1:c.423T>A	NP_001161406.1:p.Ala141=
NM_001167935.1:c.472+3921T>A	NP_001161407.1:n.472+3921T>A
NM_031443.3:c.597T>A , LRG_664t2:c.597T>A	NP_113631.1:p.Ala199=
NR_030770.1:n.679T>A
XM_006715785.2:c.486T>A	XP_006715848.1:p.Ala162=
XM_006715786.2:c.535+3921T>A	XP_006715849.1:n.535+3921T>A
XM_011515561.1:c.660T>A	XP_011513863.1:p.Ala220=
XM_011515562.1:c.597T>A	XP_011513864.1:p.Ala199=
XM_011515563.1:c.486T>A	XP_011513865.1:p.Ala162=
XM_011515564.1:c.423T>A	XP_011513866.1:p.Ala141=
XR_428088.2:n.673T>A
NM_001363458.1:c.597T>A	NP_001350387.1:p.Ala199=
NM_001363459.1:c.423T>A	NP_001350388.1:p.Ala141=
XM_006715785.4:c.486T>A	XP_006715848.1:p.Ala162=
XM_006715786.3:c.535+3921T>A	XP_006715849.1:n.535+3921T>A
XM_011515561.2:c.660T>A	XP_011513863.1:p.Ala220=
XM_011515563.3:c.486T>A	XP_011513865.1:p.Ala162=
XM_017012671.1:c.660T>A	XP_016868160.1:p.Ala220=
XM_017012672.2:c.486T>A	XP_016868161.1:p.Ala162=
XM_017012673.1:c.423T>A	XP_016868162.1:p.Ala141=
XR_428088.3:n.693T>A
NM_001363458.2:c.597T>A	NP_001350387.1:p.Ala199=
NM_001363459.2:c.423T>A	NP_001350388.1:p.Ala141=
NM_031443.4:c.597T>A MANE Select	NP_113631.1:p.Ala199=
NR_030770.2:n.679T>A
NM_001167934.2:c.423T>A	NP_001161406.1:p.Ala141=
NM_001167935.2:c.472+3921T>A	NP_001161407.1:n.472+3921T>A