Canonical Allele Identifier: CA454888188

Gene: CCM2

Linked Data

• MyVariant Identifiers: chr7:g.45108076G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068477G>T , CM000669.2:g.45068477G>T	GRCh38
NC_000007.13:g.45108076G>T , CM000669.1:g.45108076G>T	GRCh37
NC_000007.12:g.45074601G>T	NCBI36
NG_016295.1:g.73290G>T , LRG_664:g.73290G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.507G>T MANE Select	ENSP00000258781.7:p.Leu169=
ENST00000648329.1:c.507G>T	ENSP00000496916.1:p.Leu169=
ENST00000258781.10:c.507G>T	ENSP00000258781.6:p.Leu169=
ENST00000381112.7:c.570G>T	ENSP00000370503.3:p.Leu190=
ENST00000461377.5:n.860G>T
ENST00000472223.5:n.574G>T
ENST00000474617.1:c.454+3831G>T	ENSP00000419474.1:n.454+3831G>T
ENST00000475551.5:c.489G>T	ENSP00000417180.1:p.Leu163=
ENST00000477605.1:n.842G>T
ENST00000478582.5:n.684-1349G>T
ENST00000480658.5:n.335G>T
ENST00000481194.1:n.45-1349G>T
ENST00000482714.5:n.429G>T
ENST00000488727.5:c.507G>T	ENSP00000417251.1:p.Leu169=
ENST00000492883.5:n.485-1349G>T
ENST00000541586.5:c.333G>T	ENSP00000444725.1:p.Leu111=
ENST00000544363.5:c.472+3831G>T	ENSP00000438035.1:n.472+3831G>T
NM_001029835.2:c.570G>T , LRG_664t1:c.570G>T	NP_001025006.1:p.Leu190=
NM_001167934.1:c.333G>T	NP_001161406.1:p.Leu111=
NM_001167935.1:c.472+3831G>T	NP_001161407.1:n.472+3831G>T
NM_031443.3:c.507G>T , LRG_664t2:c.507G>T	NP_113631.1:p.Leu169=
NR_030770.1:n.589G>T
XM_006715785.2:c.396G>T	XP_006715848.1:p.Leu132=
XM_006715786.2:c.535+3831G>T	XP_006715849.1:n.535+3831G>T
XM_011515561.1:c.570G>T	XP_011513863.1:p.Leu190=
XM_011515562.1:c.507G>T	XP_011513864.1:p.Leu169=
XM_011515563.1:c.396G>T	XP_011513865.1:p.Leu132=
XM_011515564.1:c.333G>T	XP_011513866.1:p.Leu111=
XR_428088.2:n.583G>T
NM_001363458.1:c.507G>T	NP_001350387.1:p.Leu169=
NM_001363459.1:c.333G>T	NP_001350388.1:p.Leu111=
XM_006715785.4:c.396G>T	XP_006715848.1:p.Leu132=
XM_006715786.3:c.535+3831G>T	XP_006715849.1:n.535+3831G>T
XM_011515561.2:c.570G>T	XP_011513863.1:p.Leu190=
XM_011515563.3:c.396G>T	XP_011513865.1:p.Leu132=
XM_017012671.1:c.570G>T	XP_016868160.1:p.Leu190=
XM_017012672.2:c.396G>T	XP_016868161.1:p.Leu132=
XM_017012673.1:c.333G>T	XP_016868162.1:p.Leu111=
XR_428088.3:n.603G>T
NM_001363458.2:c.507G>T	NP_001350387.1:p.Leu169=
NM_001363459.2:c.333G>T	NP_001350388.1:p.Leu111=
NM_031443.4:c.507G>T MANE Select	NP_113631.1:p.Leu169=
NR_030770.2:n.589G>T
NM_001167934.2:c.333G>T	NP_001161406.1:p.Leu111=
NM_001167935.2:c.472+3831G>T	NP_001161407.1:n.472+3831G>T