Canonical Allele Identifier: CA157992115

Gene: CCM2

Linked Data

• dbSNP Id: rs779850799
• MyVariant Identifiers: chr7:g.45108058C>G (hg19) ; chr7:g.45068459C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068459C>G , CM000669.2:g.45068459C>G	GRCh38
NC_000007.13:g.45108058C>G , CM000669.1:g.45108058C>G	GRCh37
NC_000007.12:g.45074583C>G	NCBI36
NG_016295.1:g.73272C>G , LRG_664:g.73272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.489C>G MANE Select	ENSP00000258781.7:p.Ile163Met
ENST00000648329.1:c.489C>G	ENSP00000496916.1:p.Ile163Met
ENST00000258781.10:c.489C>G	ENSP00000258781.6:p.Ile163Met
ENST00000381112.7:c.552C>G	ENSP00000370503.3:p.Ile184Met
ENST00000461377.5:n.842C>G
ENST00000472223.5:n.556C>G
ENST00000474617.1:c.454+3813C>G	ENSP00000419474.1:n.454+3813C>G
ENST00000475551.5:c.471C>G	ENSP00000417180.1:p.Ile157Met
ENST00000477605.1:n.824C>G
ENST00000478582.5:n.684-1367C>G
ENST00000480658.5:n.317C>G
ENST00000481194.1:n.45-1367C>G
ENST00000482714.5:n.411C>G
ENST00000488727.5:c.489C>G	ENSP00000417251.1:p.Ile163Met
ENST00000492883.5:n.485-1367C>G
ENST00000541586.5:c.315C>G	ENSP00000444725.1:p.Ile105Met
ENST00000544363.5:c.472+3813C>G	ENSP00000438035.1:n.472+3813C>G
NM_001029835.2:c.552C>G , LRG_664t1:c.552C>G	NP_001025006.1:p.Ile184Met
NM_001167934.1:c.315C>G	NP_001161406.1:p.Ile105Met
NM_001167935.1:c.472+3813C>G	NP_001161407.1:n.472+3813C>G
NM_031443.3:c.489C>G , LRG_664t2:c.489C>G	NP_113631.1:p.Ile163Met
NR_030770.1:n.571C>G
XM_006715785.2:c.378C>G	XP_006715848.1:p.Ile126Met
XM_006715786.2:c.535+3813C>G	XP_006715849.1:n.535+3813C>G
XM_011515561.1:c.552C>G	XP_011513863.1:p.Ile184Met
XM_011515562.1:c.489C>G	XP_011513864.1:p.Ile163Met
XM_011515563.1:c.378C>G	XP_011513865.1:p.Ile126Met
XM_011515564.1:c.315C>G	XP_011513866.1:p.Ile105Met
XR_428088.2:n.565C>G
NM_001363458.1:c.489C>G	NP_001350387.1:p.Ile163Met
NM_001363459.1:c.315C>G	NP_001350388.1:p.Ile105Met
XM_006715785.4:c.378C>G	XP_006715848.1:p.Ile126Met
XM_006715786.3:c.535+3813C>G	XP_006715849.1:n.535+3813C>G
XM_011515561.2:c.552C>G	XP_011513863.1:p.Ile184Met
XM_011515563.3:c.378C>G	XP_011513865.1:p.Ile126Met
XM_017012671.1:c.552C>G	XP_016868160.1:p.Ile184Met
XM_017012672.2:c.378C>G	XP_016868161.1:p.Ile126Met
XM_017012673.1:c.315C>G	XP_016868162.1:p.Ile105Met
XR_428088.3:n.585C>G
NM_001363458.2:c.489C>G	NP_001350387.1:p.Ile163Met
NM_001363459.2:c.315C>G	NP_001350388.1:p.Ile105Met
NM_031443.4:c.489C>G MANE Select	NP_113631.1:p.Ile163Met
NR_030770.2:n.571C>G
NM_001167934.2:c.315C>G	NP_001161406.1:p.Ile105Met
NM_001167935.2:c.472+3813C>G	NP_001161407.1:n.472+3813C>G