Canonical Allele Identifier: CA1704061591
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45064413G= , CM000669.2:g.45064413G= GRCh38
NC_000007.13:g.45104012G= , CM000669.1:g.45104012G= GRCh37
NC_000007.12:g.45070537G= NCBI36
NG_016295.1:g.69226G= , LRG_664:g.69226G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258781.11:c.289-50G= MANE Select ENSP00000258781.7:n.289-50G=
ENST00000648329.1:c.289-50G= ENSP00000496916.1:n.289-50G=
ENST00000258781.10:c.289-50G= ENSP00000258781.6:n.289-50G=
ENST00000381112.7:c.352-50G= ENSP00000370503.3:n.352-50G=
ENST00000461377.5:n.642-50G=
ENST00000472223.5:n.356-50G=
ENST00000474617.1:c.271-50G= ENSP00000419474.1:n.271-50G=
ENST00000475551.5:c.271-50G= ENSP00000417180.1:n.271-50G=
ENST00000476594.1:n.374-50G=
ENST00000478169.5:n.511-50G=
ENST00000478582.5:n.500-50G=
ENST00000480658.5:n.301-4030G=
ENST00000482714.5:n.211-50G=
ENST00000488727.5:c.289-50G= ENSP00000417251.1:n.289-50G=
ENST00000492883.5:n.301-50G=
ENST00000541586.5:c.115-50G= ENSP00000444725.1:n.115-50G=
ENST00000544363.5:c.289-50G= ENSP00000438035.1:n.289-50G=
NM_001029835.2:c.352-50G= , LRG_664t1:c.352-50G= NP_001025006.1:n.352-50G=
NM_001167934.1:c.115-50G= NP_001161406.1:n.115-50G=
NM_001167935.1:c.289-50G= NP_001161407.1:n.289-50G=
NM_031443.3:c.289-50G= , LRG_664t2:c.289-50G= NP_113631.1:n.289-50G=
NR_030770.1:n.371-50G=
XM_006715785.2:c.178-50G= XP_006715848.1:n.178-50G=
XM_006715786.2:c.352-50G= XP_006715849.1:n.352-50G=
XM_011515561.1:c.352-50G= XP_011513863.1:n.352-50G=
XM_011515562.1:c.289-50G= XP_011513864.1:n.289-50G=
XM_011515563.1:c.178-50G= XP_011513865.1:n.178-50G=
XM_011515564.1:c.115-50G= XP_011513866.1:n.115-50G=
XR_428088.2:n.365-50G=
NM_001363458.1:c.289-50G= NP_001350387.1:n.289-50G=
NM_001363459.1:c.115-50G= NP_001350388.1:n.115-50G=
XM_006715785.4:c.178-50G= XP_006715848.1:n.178-50G=
XM_006715786.3:c.352-50G= XP_006715849.1:n.352-50G=
XM_011515561.2:c.352-50G= XP_011513863.1:n.352-50G=
XM_011515563.3:c.178-50G= XP_011513865.1:n.178-50G=
XM_017012671.1:c.352-50G= XP_016868160.1:n.352-50G=
XM_017012672.2:c.178-50G= XP_016868161.1:n.178-50G=
XM_017012673.1:c.115-50G= XP_016868162.1:n.115-50G=
XR_428088.3:n.385-50G=
NM_001363458.2:c.289-50G= NP_001350387.1:n.289-50G=
NM_001363459.2:c.115-50G= NP_001350388.1:n.115-50G=
NM_031443.4:c.289-50G= MANE Select NP_113631.1:n.289-50G=
NR_030770.2:n.371-50G=
NM_001167934.2:c.115-50G= NP_001161406.1:n.115-50G=
NM_001167935.2:c.289-50G= NP_001161407.1:n.289-50G=