Canonical Allele Identifier: CA454878132

Gene: CCM2

Linked Data

• MyVariant Identifiers: chr7:g.45077881A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038282A>G , CM000669.2:g.45038282A>G	GRCh38
NC_000007.13:g.45077881A>G , CM000669.1:g.45077881A>G	GRCh37
NC_000007.12:g.45044406A>G	NCBI36
NG_016295.1:g.43095A>G , LRG_664:g.43095A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.60A>G MANE Select	ENSP00000258781.7:p.Val20=
ENST00000648329.1:c.60A>G	ENSP00000496916.1:p.Val20=
ENST00000258781.10:c.60A>G	ENSP00000258781.6:p.Val20=
ENST00000381112.7:c.123A>G	ENSP00000370503.3:p.Val41=
ENST00000461377.5:n.413A>G
ENST00000472223.5:n.127A>G
ENST00000474617.1:c.42A>G	ENSP00000419474.1:p.Val14=
ENST00000475551.5:c.42A>G	ENSP00000417180.1:p.Val14=
ENST00000476594.1:n.22A>G
ENST00000478169.5:n.282A>G
ENST00000478582.5:n.271A>G
ENST00000480658.5:n.156A>G
ENST00000482714.5:n.126+10485A>G
ENST00000488727.5:c.60A>G	ENSP00000417251.1:p.Val20=
ENST00000492883.5:n.156A>G
ENST00000541586.5:c.31-25636A>G	ENSP00000444725.1:n.31-25636A>G
ENST00000544363.5:c.60A>G	ENSP00000438035.1:p.Val20=
NM_001029835.2:c.123A>G , LRG_664t1:c.123A>G	NP_001025006.1:p.Val41=
NM_001167934.1:c.31-25636A>G	NP_001161406.1:n.31-25636A>G
NM_001167935.1:c.60A>G	NP_001161407.1:p.Val20=
NM_031443.3:c.60A>G , LRG_664t2:c.60A>G	NP_113631.1:p.Val20=
NR_030770.1:n.142A>G
XM_006715785.2:c.93+10485A>G	XP_006715848.1:n.93+10485A>G
XM_006715786.2:c.123A>G	XP_006715849.1:p.Val41=
XM_011515561.1:c.123A>G	XP_011513863.1:p.Val41=
XM_011515562.1:c.60A>G	XP_011513864.1:p.Val20=
XM_011515563.1:c.93+10485A>G	XP_011513865.1:n.93+10485A>G
XM_011515564.1:c.31-25636A>G	XP_011513866.1:n.31-25636A>G
XR_428088.2:n.136A>G
NM_001363458.1:c.60A>G	NP_001350387.1:p.Val20=
NM_001363459.1:c.31-25636A>G	NP_001350388.1:n.31-25636A>G
XM_006715785.4:c.93+10485A>G	XP_006715848.1:n.93+10485A>G
XM_006715786.3:c.123A>G	XP_006715849.1:p.Val41=
XM_011515561.2:c.123A>G	XP_011513863.1:p.Val41=
XM_011515563.3:c.93+10485A>G	XP_011513865.1:n.93+10485A>G
XM_017012671.1:c.123A>G	XP_016868160.1:p.Val41=
XM_017012672.2:c.93+10485A>G	XP_016868161.1:n.93+10485A>G
XM_017012673.1:c.31-25636A>G	XP_016868162.1:n.31-25636A>G
XR_428088.3:n.156A>G
NM_001363458.2:c.60A>G	NP_001350387.1:p.Val20=
NM_001363459.2:c.31-25636A>G	NP_001350388.1:n.31-25636A>G
NM_031443.4:c.60A>G MANE Select	NP_113631.1:p.Val20=
NR_030770.2:n.142A>G
NM_001167934.2:c.31-25636A>G	NP_001161406.1:n.31-25636A>G
NM_001167935.2:c.60A>G	NP_001161407.1:p.Val20=