Canonical Allele Identifier: CA367426677

Gene: CCM2

Linked Data

• MyVariant Identifiers: chr7:g.45077882T>G (hg19) ; chr7:g.45038283T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038283T>G , CM000669.2:g.45038283T>G	GRCh38
NC_000007.13:g.45077882T>G , CM000669.1:g.45077882T>G	GRCh37
NC_000007.12:g.45044407T>G	NCBI36
NG_016295.1:g.43096T>G , LRG_664:g.43096T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.61T>G MANE Select	ENSP00000258781.7:p.Phe21Val
ENST00000648329.1:c.61T>G	ENSP00000496916.1:p.Phe21Val
ENST00000258781.10:c.61T>G	ENSP00000258781.6:p.Phe21Val
ENST00000381112.7:c.124T>G	ENSP00000370503.3:p.Phe42Val
ENST00000461377.5:n.414T>G
ENST00000472223.5:n.128T>G
ENST00000474617.1:c.43T>G	ENSP00000419474.1:p.Phe15Val
ENST00000475551.5:c.43T>G	ENSP00000417180.1:p.Phe15Val
ENST00000476594.1:n.23T>G
ENST00000478169.5:n.283T>G
ENST00000478582.5:n.272T>G
ENST00000480658.5:n.157T>G
ENST00000482714.5:n.126+10486T>G
ENST00000488727.5:c.61T>G	ENSP00000417251.1:p.Phe21Val
ENST00000492883.5:n.157T>G
ENST00000541586.5:c.31-25635T>G	ENSP00000444725.1:n.31-25635T>G
ENST00000544363.5:c.61T>G	ENSP00000438035.1:p.Phe21Val
NM_001029835.2:c.124T>G , LRG_664t1:c.124T>G	NP_001025006.1:p.Phe42Val
NM_001167934.1:c.31-25635T>G	NP_001161406.1:n.31-25635T>G
NM_001167935.1:c.61T>G	NP_001161407.1:p.Phe21Val
NM_031443.3:c.61T>G , LRG_664t2:c.61T>G	NP_113631.1:p.Phe21Val
NR_030770.1:n.143T>G
XM_006715785.2:c.93+10486T>G	XP_006715848.1:n.93+10486T>G
XM_006715786.2:c.124T>G	XP_006715849.1:p.Phe42Val
XM_011515561.1:c.124T>G	XP_011513863.1:p.Phe42Val
XM_011515562.1:c.61T>G	XP_011513864.1:p.Phe21Val
XM_011515563.1:c.93+10486T>G	XP_011513865.1:n.93+10486T>G
XM_011515564.1:c.31-25635T>G	XP_011513866.1:n.31-25635T>G
XR_428088.2:n.137T>G
NM_001363458.1:c.61T>G	NP_001350387.1:p.Phe21Val
NM_001363459.1:c.31-25635T>G	NP_001350388.1:n.31-25635T>G
XM_006715785.4:c.93+10486T>G	XP_006715848.1:n.93+10486T>G
XM_006715786.3:c.124T>G	XP_006715849.1:p.Phe42Val
XM_011515561.2:c.124T>G	XP_011513863.1:p.Phe42Val
XM_011515563.3:c.93+10486T>G	XP_011513865.1:n.93+10486T>G
XM_017012671.1:c.124T>G	XP_016868160.1:p.Phe42Val
XM_017012672.2:c.93+10486T>G	XP_016868161.1:n.93+10486T>G
XM_017012673.1:c.31-25635T>G	XP_016868162.1:n.31-25635T>G
XR_428088.3:n.157T>G
NM_001363458.2:c.61T>G	NP_001350387.1:p.Phe21Val
NM_001363459.2:c.31-25635T>G	NP_001350388.1:n.31-25635T>G
NM_031443.4:c.61T>G MANE Select	NP_113631.1:p.Phe21Val
NR_030770.2:n.143T>G
NM_001167934.2:c.31-25635T>G	NP_001161406.1:n.31-25635T>G
NM_001167935.2:c.61T>G	NP_001161407.1:p.Phe21Val