Canonical Allele Identifier: CA2775257684

Gene: CCM2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45000222C>G , CM000669.2:g.45000222C>G	GRCh38
NC_000007.13:g.45039821C>G , CM000669.1:g.45039821C>G	GRCh37
NC_000007.12:g.45006346C>G	NCBI36
NG_016295.1:g.5035C>G , LRG_664:g.5035C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.-112C>G MANE Select	ENSP00000258781.7:n.-112C>G
ENST00000258781.10:c.-112C>G	ENSP00000258781.6:n.-112C>G
ENST00000461377.5:n.383+365C>G
ENST00000478582.5:n.34C>G
ENST00000541586.5:c.-112C>G	ENSP00000444725.1:n.-112C>G
ENST00000544363.5:c.-112C>G	ENSP00000438035.1:n.-112C>G
NM_001167934.1:c.-112C>G	NP_001161406.1:n.-112C>G
NM_001167935.1:c.-112C>G	NP_001161407.1:n.-112C>G
NM_031443.3:c.-112C>G , LRG_664t2:c.-112C>G	NP_113631.1:n.-112C>G
NR_030770.1:n.112+365C>G
XM_011515562.1:c.-112C>G	XP_011513864.1:n.-112C>G
NM_001363458.1:c.-112C>G	NP_001350387.1:n.-112C>G
NM_001363459.1:c.-112C>G	NP_001350388.1:n.-112C>G
NM_001363458.2:c.-112C>G	NP_001350387.1:n.-112C>G
NM_001363459.2:c.-112C>G	NP_001350388.1:n.-112C>G
NM_031443.4:c.-112C>G MANE Select	NP_113631.1:n.-112C>G
NR_030770.2:n.112+365C>G
NM_001167934.2:c.-112C>G	NP_001161406.1:n.-112C>G
NM_001167935.2:c.-112C>G	NP_001161407.1:n.-112C>G