Canonical Allele Identifier: CA367430229

Gene: CCM2

Linked Data

• ClinVar Variation Id: 2742291
• ClinVar RCV Id: RCV003497596
• dbSNP Id: rs1798891223
• gnomAD v4: 7-45068457-A-G
• MyVariant Identifiers: chr7:g.45108056A>G (hg19) ; chr7:g.45068457A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068457A>G , CM000669.2:g.45068457A>G	GRCh38
NC_000007.13:g.45108056A>G , CM000669.1:g.45108056A>G	GRCh37
NC_000007.12:g.45074581A>G	NCBI36
NG_016295.1:g.73270A>G , LRG_664:g.73270A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.487A>G MANE Select	ENSP00000258781.7:p.Ile163Val
ENST00000648329.1:c.487A>G	ENSP00000496916.1:p.Ile163Val
ENST00000258781.10:c.487A>G	ENSP00000258781.6:p.Ile163Val
ENST00000381112.7:c.550A>G	ENSP00000370503.3:p.Ile184Val
ENST00000461377.5:n.840A>G
ENST00000472223.5:n.554A>G
ENST00000474617.1:c.454+3811A>G	ENSP00000419474.1:n.454+3811A>G
ENST00000475551.5:c.469A>G	ENSP00000417180.1:p.Ile157Val
ENST00000477605.1:n.822A>G
ENST00000478582.5:n.684-1369A>G
ENST00000480658.5:n.315A>G
ENST00000481194.1:n.45-1369A>G
ENST00000482714.5:n.409A>G
ENST00000488727.5:c.487A>G	ENSP00000417251.1:p.Ile163Val
ENST00000492883.5:n.485-1369A>G
ENST00000541586.5:c.313A>G	ENSP00000444725.1:p.Ile105Val
ENST00000544363.5:c.472+3811A>G	ENSP00000438035.1:n.472+3811A>G
NM_001029835.2:c.550A>G , LRG_664t1:c.550A>G	NP_001025006.1:p.Ile184Val
NM_001167934.1:c.313A>G	NP_001161406.1:p.Ile105Val
NM_001167935.1:c.472+3811A>G	NP_001161407.1:n.472+3811A>G
NM_031443.3:c.487A>G , LRG_664t2:c.487A>G	NP_113631.1:p.Ile163Val
NR_030770.1:n.569A>G
XM_006715785.2:c.376A>G	XP_006715848.1:p.Ile126Val
XM_006715786.2:c.535+3811A>G	XP_006715849.1:n.535+3811A>G
XM_011515561.1:c.550A>G	XP_011513863.1:p.Ile184Val
XM_011515562.1:c.487A>G	XP_011513864.1:p.Ile163Val
XM_011515563.1:c.376A>G	XP_011513865.1:p.Ile126Val
XM_011515564.1:c.313A>G	XP_011513866.1:p.Ile105Val
XR_428088.2:n.563A>G
NM_001363458.1:c.487A>G	NP_001350387.1:p.Ile163Val
NM_001363459.1:c.313A>G	NP_001350388.1:p.Ile105Val
XM_006715785.4:c.376A>G	XP_006715848.1:p.Ile126Val
XM_006715786.3:c.535+3811A>G	XP_006715849.1:n.535+3811A>G
XM_011515561.2:c.550A>G	XP_011513863.1:p.Ile184Val
XM_011515563.3:c.376A>G	XP_011513865.1:p.Ile126Val
XM_017012671.1:c.550A>G	XP_016868160.1:p.Ile184Val
XM_017012672.2:c.376A>G	XP_016868161.1:p.Ile126Val
XM_017012673.1:c.313A>G	XP_016868162.1:p.Ile105Val
XR_428088.3:n.583A>G
NM_001363458.2:c.487A>G	NP_001350387.1:p.Ile163Val
NM_001363459.2:c.313A>G	NP_001350388.1:p.Ile105Val
NM_031443.4:c.487A>G MANE Select	NP_113631.1:p.Ile163Val
NR_030770.2:n.569A>G
NM_001167934.2:c.313A>G	NP_001161406.1:p.Ile105Val
NM_001167935.2:c.472+3811A>G	NP_001161407.1:n.472+3811A>G