Canonical Allele Identifier: CA16043429

Gene: CCM2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45064528C>G , CM000669.2:g.45064528C>G	GRCh38
NC_000007.13:g.45104127C>G , CM000669.1:g.45104127C>G	GRCh37
NC_000007.12:g.45070652C>G	NCBI36
NG_016295.1:g.69341C>G , LRG_664:g.69341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.354C>G MANE Select	ENSP00000258781.7:p.Tyr118Ter
ENST00000648329.1:c.354C>G	ENSP00000496916.1:p.Tyr118Ter
ENST00000258781.10:c.354C>G	ENSP00000258781.6:p.Tyr118Ter
ENST00000381112.7:c.417C>G	ENSP00000370503.3:p.Tyr139Ter
ENST00000461377.5:n.707C>G
ENST00000472223.5:n.421C>G
ENST00000474617.1:c.336C>G	ENSP00000419474.1:p.Tyr112Ter
ENST00000475551.5:c.336C>G	ENSP00000417180.1:p.Tyr112Ter
ENST00000476594.1:n.439C>G
ENST00000478582.5:n.565C>G
ENST00000480658.5:n.301-3915C>G
ENST00000482714.5:n.276C>G
ENST00000488727.5:c.354C>G	ENSP00000417251.1:p.Tyr118Ter
ENST00000492883.5:n.366C>G
ENST00000541586.5:c.180C>G	ENSP00000444725.1:p.Tyr60Ter
ENST00000544363.5:c.354C>G	ENSP00000438035.1:p.Tyr118Ter
NM_001029835.2:c.417C>G , LRG_664t1:c.417C>G	NP_001025006.1:p.Tyr139Ter
NM_001167934.1:c.180C>G	NP_001161406.1:p.Tyr60Ter
NM_001167935.1:c.354C>G	NP_001161407.1:p.Tyr118Ter
NM_031443.3:c.354C>G , LRG_664t2:c.354C>G	NP_113631.1:p.Tyr118Ter
NR_030770.1:n.436C>G
XM_006715785.2:c.243C>G	XP_006715848.1:p.Tyr81Ter
XM_006715786.2:c.417C>G	XP_006715849.1:p.Tyr139Ter
XM_011515561.1:c.417C>G	XP_011513863.1:p.Tyr139Ter
XM_011515562.1:c.354C>G	XP_011513864.1:p.Tyr118Ter
XM_011515563.1:c.243C>G	XP_011513865.1:p.Tyr81Ter
XM_011515564.1:c.180C>G	XP_011513866.1:p.Tyr60Ter
XR_428088.2:n.430C>G
NM_001363458.1:c.354C>G	NP_001350387.1:p.Tyr118Ter
NM_001363459.1:c.180C>G	NP_001350388.1:p.Tyr60Ter
XM_006715785.4:c.243C>G	XP_006715848.1:p.Tyr81Ter
XM_006715786.3:c.417C>G	XP_006715849.1:p.Tyr139Ter
XM_011515561.2:c.417C>G	XP_011513863.1:p.Tyr139Ter
XM_011515563.3:c.243C>G	XP_011513865.1:p.Tyr81Ter
XM_017012671.1:c.417C>G	XP_016868160.1:p.Tyr139Ter
XM_017012672.2:c.243C>G	XP_016868161.1:p.Tyr81Ter
XM_017012673.1:c.180C>G	XP_016868162.1:p.Tyr60Ter
XR_428088.3:n.450C>G
NM_001363458.2:c.354C>G	NP_001350387.1:p.Tyr118Ter
NM_001363459.2:c.180C>G	NP_001350388.1:p.Tyr60Ter
NM_031443.4:c.354C>G MANE Select	NP_113631.1:p.Tyr118Ter
NR_030770.2:n.436C>G
NM_001167934.2:c.180C>G	NP_001161406.1:p.Tyr60Ter
NM_001167935.2:c.354C>G	NP_001161407.1:p.Tyr118Ter