Canonical Allele Identifier: CA1704063589
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45068644C= , CM000669.2:g.45068644C= GRCh38
NC_000007.13:g.45108243C= , CM000669.1:g.45108243C= GRCh37
NC_000007.12:g.45074768C= NCBI36
NG_016295.1:g.73457C= , LRG_664:g.73457C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258781.11:c.609+65C= MANE Select ENSP00000258781.7:n.609+65C=
ENST00000648329.1:c.609+65C= ENSP00000496916.1:n.609+65C=
ENST00000258781.10:c.609+65C= ENSP00000258781.6:n.609+65C=
ENST00000381112.7:c.672+65C= ENSP00000370503.3:n.672+65C=
ENST00000461377.5:n.962+65C=
ENST00000472223.5:n.676+65C=
ENST00000474617.1:c.454+3998C= ENSP00000419474.1:n.454+3998C=
ENST00000475551.5:c.591+65C= ENSP00000417180.1:n.591+65C=
ENST00000477605.1:n.944+65C=
ENST00000478582.5:n.684-1182C=
ENST00000480382.1:c.86+65C=
ENST00000480658.5:n.437+65C=
ENST00000481194.1:n.45-1182C=
ENST00000482714.5:n.531+65C=
ENST00000488727.5:c.609+65C= ENSP00000417251.1:n.609+65C=
ENST00000492883.5:n.485-1182C=
ENST00000541586.5:c.435+65C= ENSP00000444725.1:n.435+65C=
ENST00000544363.5:c.472+3998C= ENSP00000438035.1:n.472+3998C=
NM_001029835.2:c.672+65C= , LRG_664t1:c.672+65C= NP_001025006.1:n.672+65C=
NM_001167934.1:c.435+65C= NP_001161406.1:n.435+65C=
NM_001167935.1:c.472+3998C= NP_001161407.1:n.472+3998C=
NM_031443.3:c.609+65C= , LRG_664t2:c.609+65C= NP_113631.1:n.609+65C=
NR_030770.1:n.691+65C=
XM_006715785.2:c.498+65C= XP_006715848.1:n.498+65C=
XM_006715786.2:c.535+3998C= XP_006715849.1:n.535+3998C=
XM_011515561.1:c.672+65C= XP_011513863.1:n.672+65C=
XM_011515562.1:c.609+65C= XP_011513864.1:n.609+65C=
XM_011515563.1:c.498+65C= XP_011513865.1:n.498+65C=
XM_011515564.1:c.435+65C= XP_011513866.1:n.435+65C=
XR_428088.2:n.685+65C=
NM_001363458.1:c.609+65C= NP_001350387.1:n.609+65C=
NM_001363459.1:c.435+65C= NP_001350388.1:n.435+65C=
XM_006715785.4:c.498+65C= XP_006715848.1:n.498+65C=
XM_006715786.3:c.535+3998C= XP_006715849.1:n.535+3998C=
XM_011515561.2:c.672+65C= XP_011513863.1:n.672+65C=
XM_011515563.3:c.498+65C= XP_011513865.1:n.498+65C=
XM_017012671.1:c.672+65C= XP_016868160.1:n.672+65C=
XM_017012672.2:c.498+65C= XP_016868161.1:n.498+65C=
XM_017012673.1:c.435+65C= XP_016868162.1:n.435+65C=
XR_428088.3:n.705+65C=
NM_001363458.2:c.609+65C= NP_001350387.1:n.609+65C=
NM_001363459.2:c.435+65C= NP_001350388.1:n.435+65C=
NM_031443.4:c.609+65C= MANE Select NP_113631.1:n.609+65C=
NR_030770.2:n.691+65C=
NM_001167934.2:c.435+65C= NP_001161406.1:n.435+65C=
NM_001167935.2:c.472+3998C= NP_001161407.1:n.472+3998C=