Canonical Allele Identifier: CA1704041890
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45038201C= , CM000669.2:g.45038201C= GRCh38
NC_000007.13:g.45077800C= , CM000669.1:g.45077800C= GRCh37
NC_000007.12:g.45044325C= NCBI36
NG_016295.1:g.43014C= , LRG_664:g.43014C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258781.11:c.31-52C= MANE Select ENSP00000258781.7:n.31-52C=
ENST00000648329.1:c.31-52C= ENSP00000496916.1:n.31-52C=
ENST00000258781.10:c.31-52C= ENSP00000258781.6:n.31-52C=
ENST00000381112.7:c.94-52C= ENSP00000370503.3:n.94-52C=
ENST00000461377.5:n.384-52C=
ENST00000472223.5:n.98-52C=
ENST00000474617.1:c.13-52C= ENSP00000419474.1:n.13-52C=
ENST00000475551.5:c.13-52C= ENSP00000417180.1:n.13-52C=
ENST00000478169.5:n.253-52C=
ENST00000478582.5:n.242-52C=
ENST00000480658.5:n.127-52C=
ENST00000482714.5:n.126+10404C=
ENST00000488727.5:c.31-52C= ENSP00000417251.1:n.31-52C=
ENST00000492883.5:n.127-52C=
ENST00000541586.5:c.31-25717C= ENSP00000444725.1:n.31-25717C=
ENST00000544363.5:c.31-52C= ENSP00000438035.1:n.31-52C=
NM_001029835.2:c.94-52C= , LRG_664t1:c.94-52C= NP_001025006.1:n.94-52C=
NM_001167934.1:c.31-25717C= NP_001161406.1:n.31-25717C=
NM_001167935.1:c.31-52C= NP_001161407.1:n.31-52C=
NM_031443.3:c.31-52C= , LRG_664t2:c.31-52C= NP_113631.1:n.31-52C=
NR_030770.1:n.113-52C=
XM_006715785.2:c.93+10404C= XP_006715848.1:n.93+10404C=
XM_006715786.2:c.94-52C= XP_006715849.1:n.94-52C=
XM_011515561.1:c.94-52C= XP_011513863.1:n.94-52C=
XM_011515562.1:c.31-52C= XP_011513864.1:n.31-52C=
XM_011515563.1:c.93+10404C= XP_011513865.1:n.93+10404C=
XM_011515564.1:c.31-25717C= XP_011513866.1:n.31-25717C=
XR_428088.2:n.107-52C=
NM_001363458.1:c.31-52C= NP_001350387.1:n.31-52C=
NM_001363459.1:c.31-25717C= NP_001350388.1:n.31-25717C=
XM_006715785.4:c.93+10404C= XP_006715848.1:n.93+10404C=
XM_006715786.3:c.94-52C= XP_006715849.1:n.94-52C=
XM_011515561.2:c.94-52C= XP_011513863.1:n.94-52C=
XM_011515563.3:c.93+10404C= XP_011513865.1:n.93+10404C=
XM_017012671.1:c.94-52C= XP_016868160.1:n.94-52C=
XM_017012672.2:c.93+10404C= XP_016868161.1:n.93+10404C=
XM_017012673.1:c.31-25717C= XP_016868162.1:n.31-25717C=
XR_428088.3:n.127-52C=
NM_001363458.2:c.31-52C= NP_001350387.1:n.31-52C=
NM_001363459.2:c.31-25717C= NP_001350388.1:n.31-25717C=
NM_031443.4:c.31-52C= MANE Select NP_113631.1:n.31-52C=
NR_030770.2:n.113-52C=
NM_001167934.2:c.31-25717C= NP_001161406.1:n.31-25717C=
NM_001167935.2:c.31-52C= NP_001161407.1:n.31-52C=