Canonical Allele Identifier: CA367430211

Gene: CCM2

Linked Data

• MyVariant Identifiers: chr7:g.45108048A>G (hg19) ; chr7:g.45068449A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068449A>G , CM000669.2:g.45068449A>G	GRCh38
NC_000007.13:g.45108048A>G , CM000669.1:g.45108048A>G	GRCh37
NC_000007.12:g.45074573A>G	NCBI36
NG_016295.1:g.73262A>G , LRG_664:g.73262A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.479A>G MANE Select	ENSP00000258781.7:p.Asp160Gly
ENST00000648329.1:c.479A>G	ENSP00000496916.1:p.Asp160Gly
ENST00000258781.10:c.479A>G	ENSP00000258781.6:p.Asp160Gly
ENST00000381112.7:c.542A>G	ENSP00000370503.3:p.Asp181Gly
ENST00000461377.5:n.832A>G
ENST00000472223.5:n.546A>G
ENST00000474617.1:c.454+3803A>G	ENSP00000419474.1:n.454+3803A>G
ENST00000475551.5:c.461A>G	ENSP00000417180.1:p.Asp154Gly
ENST00000477605.1:n.814A>G
ENST00000478582.5:n.684-1377A>G
ENST00000480658.5:n.307A>G
ENST00000481194.1:n.45-1377A>G
ENST00000482714.5:n.401A>G
ENST00000488727.5:c.479A>G	ENSP00000417251.1:p.Asp160Gly
ENST00000492883.5:n.485-1377A>G
ENST00000541586.5:c.305A>G	ENSP00000444725.1:p.Asp102Gly
ENST00000544363.5:c.472+3803A>G	ENSP00000438035.1:n.472+3803A>G
NM_001029835.2:c.542A>G , LRG_664t1:c.542A>G	NP_001025006.1:p.Asp181Gly
NM_001167934.1:c.305A>G	NP_001161406.1:p.Asp102Gly
NM_001167935.1:c.472+3803A>G	NP_001161407.1:n.472+3803A>G
NM_031443.3:c.479A>G , LRG_664t2:c.479A>G	NP_113631.1:p.Asp160Gly
NR_030770.1:n.561A>G
XM_006715785.2:c.368A>G	XP_006715848.1:p.Asp123Gly
XM_006715786.2:c.535+3803A>G	XP_006715849.1:n.535+3803A>G
XM_011515561.1:c.542A>G	XP_011513863.1:p.Asp181Gly
XM_011515562.1:c.479A>G	XP_011513864.1:p.Asp160Gly
XM_011515563.1:c.368A>G	XP_011513865.1:p.Asp123Gly
XM_011515564.1:c.305A>G	XP_011513866.1:p.Asp102Gly
XR_428088.2:n.555A>G
NM_001363458.1:c.479A>G	NP_001350387.1:p.Asp160Gly
NM_001363459.1:c.305A>G	NP_001350388.1:p.Asp102Gly
XM_006715785.4:c.368A>G	XP_006715848.1:p.Asp123Gly
XM_006715786.3:c.535+3803A>G	XP_006715849.1:n.535+3803A>G
XM_011515561.2:c.542A>G	XP_011513863.1:p.Asp181Gly
XM_011515563.3:c.368A>G	XP_011513865.1:p.Asp123Gly
XM_017012671.1:c.542A>G	XP_016868160.1:p.Asp181Gly
XM_017012672.2:c.368A>G	XP_016868161.1:p.Asp123Gly
XM_017012673.1:c.305A>G	XP_016868162.1:p.Asp102Gly
XR_428088.3:n.575A>G
NM_001363458.2:c.479A>G	NP_001350387.1:p.Asp160Gly
NM_001363459.2:c.305A>G	NP_001350388.1:p.Asp102Gly
NM_031443.4:c.479A>G MANE Select	NP_113631.1:p.Asp160Gly
NR_030770.2:n.561A>G
NM_001167934.2:c.305A>G	NP_001161406.1:p.Asp102Gly
NM_001167935.2:c.472+3803A>G	NP_001161407.1:n.472+3803A>G