Canonical Allele Identifier: CA2682672913

Gene: CCM2

Linked Data

• gnomAD v4: 7-45000376-G-GGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45000378_45000382dup , CM000669.2:g.45000378_45000382dup	GRCh38
NC_000007.13:g.45039977_45039981dup , CM000669.1:g.45039977_45039981dup	GRCh37
NC_000007.12:g.45006502_45006506dup	NCBI36
NG_016295.1:g.5191_5195dup , LRG_664:g.5191_5195dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.30+15_30+19dup MANE Select	ENSP00000258781.7:n.30+15_30+19dup
ENST00000648329.1:c.30+15_30+19dup	ENSP00000496916.1:n.30+15_30+19dup
ENST00000258781.10:c.30+15_30+19dup	ENSP00000258781.6:n.30+15_30+19dup
ENST00000461377.5:n.383+521_383+525dup
ENST00000478582.5:n.175+15_175+19dup
ENST00000488727.5:c.30+15_30+19dup	ENSP00000417251.1:n.30+15_30+19dup
ENST00000541586.5:c.30+15_30+19dup	ENSP00000444725.1:n.30+15_30+19dup
ENST00000544363.5:c.30+15_30+19dup	ENSP00000438035.1:n.30+15_30+19dup
NM_001167934.1:c.30+15_30+19dup	NP_001161406.1:n.30+15_30+19dup
NM_001167935.1:c.30+15_30+19dup	NP_001161407.1:n.30+15_30+19dup
NM_031443.3:c.30+15_30+19dup , LRG_664t2:c.30+15_30+19dup	NP_113631.1:n.30+15_30+19dup
NR_030770.1:n.112+521_112+525dup
XM_011515562.1:c.30+15_30+19dup	XP_011513864.1:n.30+15_30+19dup
XM_011515564.1:c.30+15_30+19dup	XP_011513866.1:n.30+15_30+19dup
NM_001363458.1:c.30+15_30+19dup	NP_001350387.1:n.30+15_30+19dup
NM_001363459.1:c.30+15_30+19dup	NP_001350388.1:n.30+15_30+19dup
XM_017012673.1:c.30+15_30+19dup	XP_016868162.1:n.30+15_30+19dup
NM_001363458.2:c.30+15_30+19dup	NP_001350387.1:n.30+15_30+19dup
NM_001363459.2:c.30+15_30+19dup	NP_001350388.1:n.30+15_30+19dup
NM_031443.4:c.30+15_30+19dup MANE Select	NP_113631.1:n.30+15_30+19dup
NR_030770.2:n.112+521_112+525dup
NM_001167934.2:c.30+15_30+19dup	NP_001161406.1:n.30+15_30+19dup
NM_001167935.2:c.30+15_30+19dup	NP_001161407.1:n.30+15_30+19dup