Canonical Allele Identifier: CA16603185

Gene: CCM2

Linked Data

• ClinVar Variation Id: 376845
• ClinVar RCV Id: RCV000442431
• dbSNP Id: rs1057520070
• MyVariant Identifiers: chr7:g.45077941del (hg19) ; chr7:g.45038342del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038344del , CM000669.2:g.45038344del	GRCh38
NC_000007.13:g.45077943del , CM000669.1:g.45077943del	GRCh37
NC_000007.12:g.45044468del	NCBI36
NG_016295.1:g.43157del , LRG_664:g.43157del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.122del MANE Select	ENSP00000258781.7:p.Pro41LeufsTer19
ENST00000648329.1:c.122del	ENSP00000496916.1:p.Pro41LeufsTer19
ENST00000258781.10:c.122del	ENSP00000258781.6:p.Pro41LeufsTer19
ENST00000381112.7:c.185del	ENSP00000370503.3:p.Pro62LeufsTer19
ENST00000461377.5:n.475del
ENST00000472223.5:n.189del
ENST00000474617.1:c.104del	ENSP00000419474.1:p.Pro35LeufsTer19
ENST00000475551.5:c.104del	ENSP00000417180.1:p.Pro35LeufsTer19
ENST00000476594.1:n.84del
ENST00000478169.5:n.344del
ENST00000478582.5:n.333del
ENST00000480658.5:n.218del
ENST00000482714.5:n.126+10547del
ENST00000488727.5:c.122del	ENSP00000417251.1:p.Pro41LeufsTer19
ENST00000492883.5:n.218del
ENST00000541586.5:c.31-25574del	ENSP00000444725.1:n.31-25574del
ENST00000544363.5:c.122del	ENSP00000438035.1:p.Pro41LeufsTer19
NM_001029835.2:c.185del , LRG_664t1:c.185del	NP_001025006.1:p.Pro62LeufsTer19
NM_001167934.1:c.31-25574del	NP_001161406.1:n.31-25574del
NM_001167935.1:c.122del	NP_001161407.1:p.Pro41LeufsTer19
NM_031443.3:c.122del , LRG_664t2:c.122del	NP_113631.1:p.Pro41LeufsTer19
NR_030770.1:n.204del
XM_006715785.2:c.93+10547del	XP_006715848.1:n.93+10547del
XM_006715786.2:c.185del	XP_006715849.1:p.Pro62LeufsTer19
XM_011515561.1:c.185del	XP_011513863.1:p.Pro62LeufsTer19
XM_011515562.1:c.122del	XP_011513864.1:p.Pro41LeufsTer19
XM_011515563.1:c.93+10547del	XP_011513865.1:n.93+10547del
XM_011515564.1:c.31-25574del	XP_011513866.1:n.31-25574del
XR_428088.2:n.198del
NM_001363458.1:c.122del	NP_001350387.1:p.Pro41LeufsTer19
NM_001363459.1:c.31-25574del	NP_001350388.1:n.31-25574del
XM_006715785.4:c.93+10547del	XP_006715848.1:n.93+10547del
XM_006715786.3:c.185del	XP_006715849.1:p.Pro62LeufsTer19
XM_011515561.2:c.185del	XP_011513863.1:p.Pro62LeufsTer19
XM_011515563.3:c.93+10547del	XP_011513865.1:n.93+10547del
XM_017012671.1:c.185del	XP_016868160.1:p.Pro62LeufsTer19
XM_017012672.2:c.93+10547del	XP_016868161.1:n.93+10547del
XM_017012673.1:c.31-25574del	XP_016868162.1:n.31-25574del
XR_428088.3:n.218del
NM_001363458.2:c.122del	NP_001350387.1:p.Pro41LeufsTer19
NM_001363459.2:c.31-25574del	NP_001350388.1:n.31-25574del
NM_031443.4:c.122del MANE Select	NP_113631.1:p.Pro41LeufsTer19
NR_030770.2:n.204del
NM_001167934.2:c.31-25574del	NP_001161406.1:n.31-25574del
NM_001167935.2:c.122del	NP_001161407.1:p.Pro41LeufsTer19