Canonical Allele Identifier: CA1704042120
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45038376C= , CM000669.2:g.45038376C= GRCh38
NC_000007.13:g.45077975C= , CM000669.1:g.45077975C= GRCh37
NC_000007.12:g.45044500C= NCBI36
NG_016295.1:g.43189C= , LRG_664:g.43189C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258781.11:c.154C= MANE Select ENSP00000258781.7:p.Arg52=
ENST00000648329.1:c.154C= ENSP00000496916.1:p.Arg52=
ENST00000258781.10:c.154C= ENSP00000258781.6:p.Arg52=
ENST00000381112.7:c.217C= ENSP00000370503.3:p.Arg73=
ENST00000461377.5:n.507C=
ENST00000472223.5:n.221C=
ENST00000474617.1:c.136C= ENSP00000419474.1:p.Arg46=
ENST00000475551.5:c.136C= ENSP00000417180.1:p.Arg46=
ENST00000476594.1:n.116C=
ENST00000478169.5:n.376C=
ENST00000478582.5:n.365C=
ENST00000480658.5:n.250C=
ENST00000482714.5:n.126+10579C=
ENST00000488727.5:c.154C= ENSP00000417251.1:p.Arg52=
ENST00000492883.5:n.250C=
ENST00000541586.5:c.31-25542C= ENSP00000444725.1:n.31-25542C=
ENST00000544363.5:c.154C= ENSP00000438035.1:p.Arg52=
NM_001029835.2:c.217C= , LRG_664t1:c.217C= NP_001025006.1:p.Arg73=
NM_001167934.1:c.31-25542C= NP_001161406.1:n.31-25542C=
NM_001167935.1:c.154C= NP_001161407.1:p.Arg52=
NM_031443.3:c.154C= , LRG_664t2:c.154C= NP_113631.1:p.Arg52=
NR_030770.1:n.236C=
XM_006715785.2:c.93+10579C= XP_006715848.1:n.93+10579C=
XM_006715786.2:c.217C= XP_006715849.1:p.Arg73=
XM_011515561.1:c.217C= XP_011513863.1:p.Arg73=
XM_011515562.1:c.154C= XP_011513864.1:p.Arg52=
XM_011515563.1:c.93+10579C= XP_011513865.1:n.93+10579C=
XM_011515564.1:c.31-25542C= XP_011513866.1:n.31-25542C=
XR_428088.2:n.230C=
NM_001363458.1:c.154C= NP_001350387.1:p.Arg52=
NM_001363459.1:c.31-25542C= NP_001350388.1:n.31-25542C=
XM_006715785.4:c.93+10579C= XP_006715848.1:n.93+10579C=
XM_006715786.3:c.217C= XP_006715849.1:p.Arg73=
XM_011515561.2:c.217C= XP_011513863.1:p.Arg73=
XM_011515563.3:c.93+10579C= XP_011513865.1:n.93+10579C=
XM_017012671.1:c.217C= XP_016868160.1:p.Arg73=
XM_017012672.2:c.93+10579C= XP_016868161.1:n.93+10579C=
XM_017012673.1:c.31-25542C= XP_016868162.1:n.31-25542C=
XR_428088.3:n.250C=
NM_001363458.2:c.154C= NP_001350387.1:p.Arg52=
NM_001363459.2:c.31-25542C= NP_001350388.1:n.31-25542C=
NM_031443.4:c.154C= MANE Select NP_113631.1:p.Arg52=
NR_030770.2:n.236C=
NM_001167934.2:c.31-25542C= NP_001161406.1:n.31-25542C=
NM_001167935.2:c.154C= NP_001161407.1:p.Arg52=