Canonical Allele Identifier: CA2682675118

Gene: CCM2

Linked Data

• gnomAD v4: 7-45038467-AGTGACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45038470_45038475del , CM000669.2:g.45038470_45038475del	GRCh38
NC_000007.13:g.45078069_45078074del , CM000669.1:g.45078069_45078074del	GRCh37
NC_000007.12:g.45044594_45044599del	NCBI36
NG_016295.1:g.43283_43288del , LRG_664:g.43283_43288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.204+44_204+49del MANE Select	ENSP00000258781.7:n.204+44_204+49del
ENST00000648329.1:c.204+44_204+49del	ENSP00000496916.1:n.204+44_204+49del
ENST00000258781.10:c.204+44_204+49del	ENSP00000258781.6:n.204+44_204+49del
ENST00000381112.7:c.267+44_267+49del	ENSP00000370503.3:n.267+44_267+49del
ENST00000461377.5:n.557+44_557+49del
ENST00000472223.5:n.271+44_271+49del
ENST00000474617.1:c.186+44_186+49del	ENSP00000419474.1:n.186+44_186+49del
ENST00000475551.5:c.186+44_186+49del	ENSP00000417180.1:n.186+44_186+49del
ENST00000476594.1:n.166+44_166+49del
ENST00000478169.5:n.426+44_426+49del
ENST00000478582.5:n.415+44_415+49del
ENST00000480658.5:n.300+44_300+49del
ENST00000482714.5:n.126+10673_126+10678del
ENST00000488727.5:c.204+44_204+49del	ENSP00000417251.1:n.204+44_204+49del
ENST00000492883.5:n.300+44_300+49del
ENST00000541586.5:c.31-25448_31-25443del	ENSP00000444725.1:n.31-25448_31-25443del
ENST00000544363.5:c.204+44_204+49del	ENSP00000438035.1:n.204+44_204+49del
NM_001029835.2:c.267+44_267+49del , LRG_664t1:c.267+44_267+49del	NP_001025006.1:n.267+44_267+49del
NM_001167934.1:c.31-25448_31-25443del	NP_001161406.1:n.31-25448_31-25443del
NM_001167935.1:c.204+44_204+49del	NP_001161407.1:n.204+44_204+49del
NM_031443.3:c.204+44_204+49del , LRG_664t2:c.204+44_204+49del	NP_113631.1:n.204+44_204+49del
NR_030770.1:n.286+44_286+49del
XM_006715785.2:c.93+10673_93+10678del	XP_006715848.1:n.93+10673_93+10678del
XM_006715786.2:c.267+44_267+49del	XP_006715849.1:n.267+44_267+49del
XM_011515561.1:c.267+44_267+49del	XP_011513863.1:n.267+44_267+49del
XM_011515562.1:c.204+44_204+49del	XP_011513864.1:n.204+44_204+49del
XM_011515563.1:c.93+10673_93+10678del	XP_011513865.1:n.93+10673_93+10678del
XM_011515564.1:c.31-25448_31-25443del	XP_011513866.1:n.31-25448_31-25443del
XR_428088.2:n.280+44_280+49del
NM_001363458.1:c.204+44_204+49del	NP_001350387.1:n.204+44_204+49del
NM_001363459.1:c.31-25448_31-25443del	NP_001350388.1:n.31-25448_31-25443del
XM_006715785.4:c.93+10673_93+10678del	XP_006715848.1:n.93+10673_93+10678del
XM_006715786.3:c.267+44_267+49del	XP_006715849.1:n.267+44_267+49del
XM_011515561.2:c.267+44_267+49del	XP_011513863.1:n.267+44_267+49del
XM_011515563.3:c.93+10673_93+10678del	XP_011513865.1:n.93+10673_93+10678del
XM_017012671.1:c.267+44_267+49del	XP_016868160.1:n.267+44_267+49del
XM_017012672.2:c.93+10673_93+10678del	XP_016868161.1:n.93+10673_93+10678del
XM_017012673.1:c.31-25448_31-25443del	XP_016868162.1:n.31-25448_31-25443del
XR_428088.3:n.300+44_300+49del
NM_001363458.2:c.204+44_204+49del	NP_001350387.1:n.204+44_204+49del
NM_001363459.2:c.31-25448_31-25443del	NP_001350388.1:n.31-25448_31-25443del
NM_031443.4:c.204+44_204+49del MANE Select	NP_113631.1:n.204+44_204+49del
NR_030770.2:n.286+44_286+49del
NM_001167934.2:c.31-25448_31-25443del	NP_001161406.1:n.31-25448_31-25443del
NM_001167935.2:c.204+44_204+49del	NP_001161407.1:n.204+44_204+49del