Canonical Allele Identifier: CA1704061624
Gene: CCM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.45064477T= , CM000669.2:g.45064477T= GRCh38
NC_000007.13:g.45104076T= , CM000669.1:g.45104076T= GRCh37
NC_000007.12:g.45070601T= NCBI36
NG_016295.1:g.69290T= , LRG_664:g.69290T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258781.11:c.303T= MANE Select ENSP00000258781.7:p.Leu101=
ENST00000648329.1:c.303T= ENSP00000496916.1:p.Leu101=
ENST00000258781.10:c.303T= ENSP00000258781.6:p.Leu101=
ENST00000381112.7:c.366T= ENSP00000370503.3:p.Leu122=
ENST00000461377.5:n.656T=
ENST00000472223.5:n.370T=
ENST00000474617.1:c.285T= ENSP00000419474.1:p.Leu95=
ENST00000475551.5:c.285T= ENSP00000417180.1:p.Leu95=
ENST00000476594.1:n.388T=
ENST00000478169.5:n.525T=
ENST00000478582.5:n.514T=
ENST00000480658.5:n.301-3966T=
ENST00000482714.5:n.225T=
ENST00000488727.5:c.303T= ENSP00000417251.1:p.Leu101=
ENST00000492883.5:n.315T=
ENST00000541586.5:c.129T= ENSP00000444725.1:p.Leu43=
ENST00000544363.5:c.303T= ENSP00000438035.1:p.Leu101=
NM_001029835.2:c.366T= , LRG_664t1:c.366T= NP_001025006.1:p.Leu122=
NM_001167934.1:c.129T= NP_001161406.1:p.Leu43=
NM_001167935.1:c.303T= NP_001161407.1:p.Leu101=
NM_031443.3:c.303T= , LRG_664t2:c.303T= NP_113631.1:p.Leu101=
NR_030770.1:n.385T=
XM_006715785.2:c.192T= XP_006715848.1:p.Leu64=
XM_006715786.2:c.366T= XP_006715849.1:p.Leu122=
XM_011515561.1:c.366T= XP_011513863.1:p.Leu122=
XM_011515562.1:c.303T= XP_011513864.1:p.Leu101=
XM_011515563.1:c.192T= XP_011513865.1:p.Leu64=
XM_011515564.1:c.129T= XP_011513866.1:p.Leu43=
XR_428088.2:n.379T=
NM_001363458.1:c.303T= NP_001350387.1:p.Leu101=
NM_001363459.1:c.129T= NP_001350388.1:p.Leu43=
XM_006715785.4:c.192T= XP_006715848.1:p.Leu64=
XM_006715786.3:c.366T= XP_006715849.1:p.Leu122=
XM_011515561.2:c.366T= XP_011513863.1:p.Leu122=
XM_011515563.3:c.192T= XP_011513865.1:p.Leu64=
XM_017012671.1:c.366T= XP_016868160.1:p.Leu122=
XM_017012672.2:c.192T= XP_016868161.1:p.Leu64=
XM_017012673.1:c.129T= XP_016868162.1:p.Leu43=
XR_428088.3:n.399T=
NM_001363458.2:c.303T= NP_001350387.1:p.Leu101=
NM_001363459.2:c.129T= NP_001350388.1:p.Leu43=
NM_031443.4:c.303T= MANE Select NP_113631.1:p.Leu101=
NR_030770.2:n.385T=
NM_001167934.2:c.129T= NP_001161406.1:p.Leu43=
NM_001167935.2:c.303T= NP_001161407.1:p.Leu101=