Canonical Allele Identifier: CA1704063568

Gene: CCM2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068601T= , CM000669.2:g.45068601T=	GRCh38
NC_000007.13:g.45108200T= , CM000669.1:g.45108200T=	GRCh37
NC_000007.12:g.45074725T=	NCBI36
NG_016295.1:g.73414T= , LRG_664:g.73414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.609+22T= MANE Select	ENSP00000258781.7:n.609+22T=
ENST00000648329.1:c.609+22T=	ENSP00000496916.1:n.609+22T=
ENST00000258781.10:c.609+22T=	ENSP00000258781.6:n.609+22T=
ENST00000381112.7:c.672+22T=	ENSP00000370503.3:n.672+22T=
ENST00000461377.5:n.962+22T=
ENST00000472223.5:n.676+22T=
ENST00000474617.1:c.454+3955T=	ENSP00000419474.1:n.454+3955T=
ENST00000475551.5:c.591+22T=	ENSP00000417180.1:n.591+22T=
ENST00000477605.1:n.944+22T=
ENST00000478582.5:n.684-1225T=
ENST00000480382.1:c.86+22T=
ENST00000480658.5:n.437+22T=
ENST00000481194.1:n.45-1225T=
ENST00000482714.5:n.531+22T=
ENST00000488727.5:c.609+22T=	ENSP00000417251.1:n.609+22T=
ENST00000492883.5:n.485-1225T=
ENST00000541586.5:c.435+22T=	ENSP00000444725.1:n.435+22T=
ENST00000544363.5:c.472+3955T=	ENSP00000438035.1:n.472+3955T=
NM_001029835.2:c.672+22T= , LRG_664t1:c.672+22T=	NP_001025006.1:n.672+22T=
NM_001167934.1:c.435+22T=	NP_001161406.1:n.435+22T=
NM_001167935.1:c.472+3955T=	NP_001161407.1:n.472+3955T=
NM_031443.3:c.609+22T= , LRG_664t2:c.609+22T=	NP_113631.1:n.609+22T=
NR_030770.1:n.691+22T=
XM_006715785.2:c.498+22T=	XP_006715848.1:n.498+22T=
XM_006715786.2:c.535+3955T=	XP_006715849.1:n.535+3955T=
XM_011515561.1:c.672+22T=	XP_011513863.1:n.672+22T=
XM_011515562.1:c.609+22T=	XP_011513864.1:n.609+22T=
XM_011515563.1:c.498+22T=	XP_011513865.1:n.498+22T=
XM_011515564.1:c.435+22T=	XP_011513866.1:n.435+22T=
XR_428088.2:n.685+22T=
NM_001363458.1:c.609+22T=	NP_001350387.1:n.609+22T=
NM_001363459.1:c.435+22T=	NP_001350388.1:n.435+22T=
XM_006715785.4:c.498+22T=	XP_006715848.1:n.498+22T=
XM_006715786.3:c.535+3955T=	XP_006715849.1:n.535+3955T=
XM_011515561.2:c.672+22T=	XP_011513863.1:n.672+22T=
XM_011515563.3:c.498+22T=	XP_011513865.1:n.498+22T=
XM_017012671.1:c.672+22T=	XP_016868160.1:n.672+22T=
XM_017012672.2:c.498+22T=	XP_016868161.1:n.498+22T=
XM_017012673.1:c.435+22T=	XP_016868162.1:n.435+22T=
XR_428088.3:n.705+22T=
NM_001363458.2:c.609+22T=	NP_001350387.1:n.609+22T=
NM_001363459.2:c.435+22T=	NP_001350388.1:n.435+22T=
NM_031443.4:c.609+22T= MANE Select	NP_113631.1:n.609+22T=
NR_030770.2:n.691+22T=
NM_001167934.2:c.435+22T=	NP_001161406.1:n.435+22T=
NM_001167935.2:c.472+3955T=	NP_001161407.1:n.472+3955T=