Canonical Allele Identifier: CA2682677661

Gene: CCM2

Linked Data

• gnomAD v4: 7-45068661-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45068664_45068665del , CM000669.2:g.45068664_45068665del	GRCh38
NC_000007.13:g.45108263_45108264del , CM000669.1:g.45108263_45108264del	GRCh37
NC_000007.12:g.45074788_45074789del	NCBI36
NG_016295.1:g.73477_73478del , LRG_664:g.73477_73478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.609+85_609+86del MANE Select	ENSP00000258781.7:n.609+85_609+86del
ENST00000648329.1:c.609+85_609+86del	ENSP00000496916.1:n.609+85_609+86del
ENST00000258781.10:c.609+85_609+86del	ENSP00000258781.6:n.609+85_609+86del
ENST00000381112.7:c.672+85_672+86del	ENSP00000370503.3:n.672+85_672+86del
ENST00000461377.5:n.962+85_962+86del
ENST00000472223.5:n.676+85_676+86del
ENST00000474617.1:c.454+4018_454+4019del	ENSP00000419474.1:n.454+4018_454+4019del
ENST00000475551.5:c.591+85_591+86del	ENSP00000417180.1:n.591+85_591+86del
ENST00000477605.1:n.944+85_944+86del
ENST00000478582.5:n.684-1162_684-1161del
ENST00000480382.1:c.86+85_86+86del
ENST00000480658.5:n.437+85_437+86del
ENST00000481194.1:n.45-1162_45-1161del
ENST00000482714.5:n.531+85_531+86del
ENST00000488727.5:c.609+85_609+86del	ENSP00000417251.1:n.609+85_609+86del
ENST00000492883.5:n.485-1162_485-1161del
ENST00000541586.5:c.435+85_435+86del	ENSP00000444725.1:n.435+85_435+86del
ENST00000544363.5:c.472+4018_472+4019del	ENSP00000438035.1:n.472+4018_472+4019del
NM_001029835.2:c.672+85_672+86del , LRG_664t1:c.672+85_672+86del	NP_001025006.1:n.672+85_672+86del
NM_001167934.1:c.435+85_435+86del	NP_001161406.1:n.435+85_435+86del
NM_001167935.1:c.472+4018_472+4019del	NP_001161407.1:n.472+4018_472+4019del
NM_031443.3:c.609+85_609+86del , LRG_664t2:c.609+85_609+86del	NP_113631.1:n.609+85_609+86del
NR_030770.1:n.691+85_691+86del
XM_006715785.2:c.498+85_498+86del	XP_006715848.1:n.498+85_498+86del
XM_006715786.2:c.535+4018_535+4019del	XP_006715849.1:n.535+4018_535+4019del
XM_011515561.1:c.672+85_672+86del	XP_011513863.1:n.672+85_672+86del
XM_011515562.1:c.609+85_609+86del	XP_011513864.1:n.609+85_609+86del
XM_011515563.1:c.498+85_498+86del	XP_011513865.1:n.498+85_498+86del
XM_011515564.1:c.435+85_435+86del	XP_011513866.1:n.435+85_435+86del
XR_428088.2:n.685+85_685+86del
NM_001363458.1:c.609+85_609+86del	NP_001350387.1:n.609+85_609+86del
NM_001363459.1:c.435+85_435+86del	NP_001350388.1:n.435+85_435+86del
XM_006715785.4:c.498+85_498+86del	XP_006715848.1:n.498+85_498+86del
XM_006715786.3:c.535+4018_535+4019del	XP_006715849.1:n.535+4018_535+4019del
XM_011515561.2:c.672+85_672+86del	XP_011513863.1:n.672+85_672+86del
XM_011515563.3:c.498+85_498+86del	XP_011513865.1:n.498+85_498+86del
XM_017012671.1:c.672+85_672+86del	XP_016868160.1:n.672+85_672+86del
XM_017012672.2:c.498+85_498+86del	XP_016868161.1:n.498+85_498+86del
XM_017012673.1:c.435+85_435+86del	XP_016868162.1:n.435+85_435+86del
XR_428088.3:n.705+85_705+86del
NM_001363458.2:c.609+85_609+86del	NP_001350387.1:n.609+85_609+86del
NM_001363459.2:c.435+85_435+86del	NP_001350388.1:n.435+85_435+86del
NM_031443.4:c.609+85_609+86del MANE Select	NP_113631.1:n.609+85_609+86del
NR_030770.2:n.691+85_691+86del
NM_001167934.2:c.435+85_435+86del	NP_001161406.1:n.435+85_435+86del
NM_001167935.2:c.472+4018_472+4019del	NP_001161407.1:n.472+4018_472+4019del