Canonical Allele Identifier: CA915944922

Gene: CCM2

Linked Data

• ClinVar Variation Id: 804670
• ClinVar RCV Id: RCV000991754
• dbSNP Id: rs1583901813

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038320_45038345del , CM000669.2:g.45038320_45038345del	GRCh38
NC_000007.13:g.45077919_45077944del , CM000669.1:g.45077919_45077944del	GRCh37
NC_000007.12:g.45044444_45044469del	NCBI36
NG_016295.1:g.43133_43158del , LRG_664:g.43133_43158del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.98_123del MANE Select	ENSP00000258781.7:p.His33ProfsTer10
ENST00000648329.1:c.98_123del	ENSP00000496916.1:p.His33ProfsTer10
ENST00000258781.10:c.98_123del	ENSP00000258781.6:p.His33ProfsTer10
ENST00000381112.7:c.161_186del	ENSP00000370503.3:p.His54ProfsTer10
ENST00000461377.5:n.451_476del
ENST00000472223.5:n.165_190del
ENST00000474617.1:c.80_105del	ENSP00000419474.1:p.His27ProfsTer10
ENST00000475551.5:c.80_105del	ENSP00000417180.1:p.His27ProfsTer10
ENST00000476594.1:n.60_85del
ENST00000478169.5:n.320_345del
ENST00000478582.5:n.309_334del
ENST00000480658.5:n.194_219del
ENST00000482714.5:n.126+10523_126+10548del
ENST00000488727.5:c.98_123del	ENSP00000417251.1:p.His33ProfsTer10
ENST00000492883.5:n.194_219del
ENST00000541586.5:c.31-25598_31-25573del	ENSP00000444725.1:n.31-25598_31-25573del
ENST00000544363.5:c.98_123del	ENSP00000438035.1:p.His33ProfsTer10
NM_001029835.2:c.161_186del , LRG_664t1:c.161_186del	NP_001025006.1:p.His54ProfsTer10
NM_001167934.1:c.31-25598_31-25573del	NP_001161406.1:n.31-25598_31-25573del
NM_001167935.1:c.98_123del	NP_001161407.1:p.His33ProfsTer10
NM_031443.3:c.98_123del , LRG_664t2:c.98_123del	NP_113631.1:p.His33ProfsTer10
NR_030770.1:n.180_205del
XM_006715785.2:c.93+10523_93+10548del	XP_006715848.1:n.93+10523_93+10548del
XM_006715786.2:c.161_186del	XP_006715849.1:p.His54ProfsTer10
XM_011515561.1:c.161_186del	XP_011513863.1:p.His54ProfsTer10
XM_011515562.1:c.98_123del	XP_011513864.1:p.His33ProfsTer10
XM_011515563.1:c.93+10523_93+10548del	XP_011513865.1:n.93+10523_93+10548del
XM_011515564.1:c.31-25598_31-25573del	XP_011513866.1:n.31-25598_31-25573del
XR_428088.2:n.174_199del
NM_001363458.1:c.98_123del	NP_001350387.1:p.His33ProfsTer10
NM_001363459.1:c.31-25598_31-25573del	NP_001350388.1:n.31-25598_31-25573del
XM_006715785.4:c.93+10523_93+10548del	XP_006715848.1:n.93+10523_93+10548del
XM_006715786.3:c.161_186del	XP_006715849.1:p.His54ProfsTer10
XM_011515561.2:c.161_186del	XP_011513863.1:p.His54ProfsTer10
XM_011515563.3:c.93+10523_93+10548del	XP_011513865.1:n.93+10523_93+10548del
XM_017012671.1:c.161_186del	XP_016868160.1:p.His54ProfsTer10
XM_017012672.2:c.93+10523_93+10548del	XP_016868161.1:n.93+10523_93+10548del
XM_017012673.1:c.31-25598_31-25573del	XP_016868162.1:n.31-25598_31-25573del
XR_428088.3:n.194_219del
NM_001363458.2:c.98_123del	NP_001350387.1:p.His33ProfsTer10
NM_001363459.2:c.31-25598_31-25573del	NP_001350388.1:n.31-25598_31-25573del
NM_031443.4:c.98_123del MANE Select	NP_113631.1:p.His33ProfsTer10
NR_030770.2:n.180_205del
NM_001167934.2:c.31-25598_31-25573del	NP_001161406.1:n.31-25598_31-25573del
NM_001167935.2:c.98_123del	NP_001161407.1:p.His33ProfsTer10