Canonical Allele Identifier: CA1704022527
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45000272G= , CM000669.2:g.45000272G= GRCh38
NC_000007.13:g.45039871G= , CM000669.1:g.45039871G= GRCh37
NC_000007.12:g.45006396G= NCBI36
NG_016295.1:g.5085G= , LRG_664:g.5085G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258781.11:c.-62G= MANE Select ENSP00000258781.7:n.-62G=
ENST00000258781.10:c.-62G= ENSP00000258781.6:n.-62G=
ENST00000461377.5:n.383+415G=
ENST00000478582.5:n.84G=
ENST00000488727.5:c.-62G= ENSP00000417251.1:n.-62G=
ENST00000541586.5:c.-62G= ENSP00000444725.1:n.-62G=
ENST00000544363.5:c.-62G= ENSP00000438035.1:n.-62G=
NM_001167934.1:c.-62G= NP_001161406.1:n.-62G=
NM_001167935.1:c.-62G= NP_001161407.1:n.-62G=
NM_031443.3:c.-62G= , LRG_664t2:c.-62G= NP_113631.1:n.-62G=
NR_030770.1:n.112+415G=
XM_011515562.1:c.-62G= XP_011513864.1:n.-62G=
XM_011515564.1:c.-62G= XP_011513866.1:n.-62G=
NM_001363458.1:c.-62G= NP_001350387.1:n.-62G=
NM_001363459.1:c.-62G= NP_001350388.1:n.-62G=
XM_017012673.1:c.-62G= XP_016868162.1:n.-62G=
NM_001363458.2:c.-62G= NP_001350387.1:n.-62G=
NM_001363459.2:c.-62G= NP_001350388.1:n.-62G=
NM_031443.4:c.-62G= MANE Select NP_113631.1:n.-62G=
NR_030770.2:n.112+415G=
NM_001167934.2:c.-62G= NP_001161406.1:n.-62G=
NM_001167935.2:c.-62G= NP_001161407.1:n.-62G=