Canonical Allele Identifier: CA1704063502
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45068468C= , CM000669.2:g.45068468C= GRCh38
NC_000007.13:g.45108067C= , CM000669.1:g.45108067C= GRCh37
NC_000007.12:g.45074592C= NCBI36
NG_016295.1:g.73281C= , LRG_664:g.73281C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258781.11:c.498C= MANE Select ENSP00000258781.7:p.Ser166=
ENST00000648329.1:c.498C= ENSP00000496916.1:p.Ser166=
ENST00000258781.10:c.498C= ENSP00000258781.6:p.Ser166=
ENST00000381112.7:c.561C= ENSP00000370503.3:p.Ser187=
ENST00000461377.5:n.851C=
ENST00000472223.5:n.565C=
ENST00000474617.1:c.454+3822C= ENSP00000419474.1:n.454+3822C=
ENST00000475551.5:c.480C= ENSP00000417180.1:p.Ser160=
ENST00000477605.1:n.833C=
ENST00000478582.5:n.684-1358C=
ENST00000480658.5:n.326C=
ENST00000481194.1:n.45-1358C=
ENST00000482714.5:n.420C=
ENST00000488727.5:c.498C= ENSP00000417251.1:p.Ser166=
ENST00000492883.5:n.485-1358C=
ENST00000541586.5:c.324C= ENSP00000444725.1:p.Ser108=
ENST00000544363.5:c.472+3822C= ENSP00000438035.1:n.472+3822C=
NM_001029835.2:c.561C= , LRG_664t1:c.561C= NP_001025006.1:p.Ser187=
NM_001167934.1:c.324C= NP_001161406.1:p.Ser108=
NM_001167935.1:c.472+3822C= NP_001161407.1:n.472+3822C=
NM_031443.3:c.498C= , LRG_664t2:c.498C= NP_113631.1:p.Ser166=
NR_030770.1:n.580C=
XM_006715785.2:c.387C= XP_006715848.1:p.Ser129=
XM_006715786.2:c.535+3822C= XP_006715849.1:n.535+3822C=
XM_011515561.1:c.561C= XP_011513863.1:p.Ser187=
XM_011515562.1:c.498C= XP_011513864.1:p.Ser166=
XM_011515563.1:c.387C= XP_011513865.1:p.Ser129=
XM_011515564.1:c.324C= XP_011513866.1:p.Ser108=
XR_428088.2:n.574C=
NM_001363458.1:c.498C= NP_001350387.1:p.Ser166=
NM_001363459.1:c.324C= NP_001350388.1:p.Ser108=
XM_006715785.4:c.387C= XP_006715848.1:p.Ser129=
XM_006715786.3:c.535+3822C= XP_006715849.1:n.535+3822C=
XM_011515561.2:c.561C= XP_011513863.1:p.Ser187=
XM_011515563.3:c.387C= XP_011513865.1:p.Ser129=
XM_017012671.1:c.561C= XP_016868160.1:p.Ser187=
XM_017012672.2:c.387C= XP_016868161.1:p.Ser129=
XM_017012673.1:c.324C= XP_016868162.1:p.Ser108=
XR_428088.3:n.594C=
NM_001363458.2:c.498C= NP_001350387.1:p.Ser166=
NM_001363459.2:c.324C= NP_001350388.1:p.Ser108=
NM_031443.4:c.498C= MANE Select NP_113631.1:p.Ser166=
NR_030770.2:n.580C=
NM_001167934.2:c.324C= NP_001161406.1:p.Ser108=
NM_001167935.2:c.472+3822C= NP_001161407.1:n.472+3822C=