Canonical Allele Identifier: CA1539651007
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37153786T= , CM000667.2:g.37153786T= GRCh38
NC_000005.9:g.37153888T= , CM000667.1:g.37153888T= GRCh37
NC_000005.8:g.37189645T= NCBI36
NG_032772.1:g.100643A=
NG_032772.2:g.100643A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1326A=
ENST00000651892.2:c.8327A= MANE Select ENSP00000498265.2:p.Glu2776=
ENST00000425232.6:c.8165A= ENSP00000389014.2:p.Glu2722=
ENST00000508244.5:c.8165A= ENSP00000421690.1:p.Glu2722=
ENST00000508405.1:n.59A=
ENST00000509849.5:c.5339A= ENSP00000426337.1:p.Glu1780=
ENST00000509957.5:n.569A=
ENST00000511824.2:c.1441A=
ENST00000514429.5:c.5363A= ENSP00000424223.1:p.Glu1788=
NM_023073.3:c.8165A= NP_075561.3:p.Glu2722=
XM_005248345.2:c.8327A= XP_005248402.1:p.Glu2776=
XM_005248346.2:c.8324A= XP_005248403.1:p.Glu2775=
XM_005248347.2:c.8324A= XP_005248404.1:p.Glu2775=
XM_005248349.2:c.8216A= XP_005248406.1:p.Glu2739=
XM_005248350.2:c.8198A= XP_005248407.1:p.Glu2733=
XM_005248353.3:c.4970A= XP_005248410.1:p.Glu1657=
XM_006714489.2:c.8327A= XP_006714552.1:p.Glu2776=
XM_006714491.2:c.2900A= XP_006714554.1:p.Glu967=
XM_011514085.1:c.8327A= XP_011512387.1:p.Glu2776=
XM_011514086.1:c.8327A= XP_011512388.1:p.Glu2776=
XM_011514087.1:c.8273A= XP_011512389.1:p.Glu2758=
XM_011514088.1:c.8219A= XP_011512390.1:p.Glu2740=
XM_011514089.1:c.8327A= XP_011512391.1:p.Glu2776=
XM_011514090.1:c.8009A= XP_011512392.1:p.Glu2670=
XM_011514091.1:c.7655A= XP_011512393.1:p.Glu2552=
XM_011514092.1:c.8327A= XP_011512394.1:p.Glu2776=
XM_011514094.1:c.5552A= XP_011512396.1:p.Glu1851=
XR_427661.2:n.8502A=
XR_925644.1:n.8502A=
XM_005248345.4:c.8327A= XP_005248402.1:p.Glu2776=
XM_005248346.4:c.8324A= XP_005248403.1:p.Glu2775=
XM_005248347.4:c.8324A= XP_005248404.1:p.Glu2775=
XM_005248349.4:c.8216A= XP_005248406.1:p.Glu2739=
XM_005248350.4:c.8198A= XP_005248407.1:p.Glu2733=
XM_006714491.3:c.2900A= XP_006714554.1:p.Glu967=
XM_011514085.3:c.8327A= XP_011512387.1:p.Glu2776=
XM_011514086.3:c.8327A= XP_011512388.1:p.Glu2776=
XM_011514087.2:c.8273A= XP_011512389.1:p.Glu2758=
XM_011514088.2:c.8219A= XP_011512390.1:p.Glu2740=
XM_011514089.2:c.8327A= XP_011512391.1:p.Glu2776=
XM_011514090.3:c.8009A= XP_011512392.1:p.Glu2670=
XM_011514092.2:c.8327A= XP_011512394.1:p.Glu2776=
XM_011514094.2:c.5552A= XP_011512396.1:p.Glu1851=
XM_017009760.1:c.8138A= XP_016865249.1:p.Glu2713=
XM_017009761.2:c.8138A= XP_016865250.1:p.Glu2713=
XM_017009763.1:c.7334A= XP_016865252.1:p.Glu2445=
XM_017009765.1:c.7139A= XP_016865254.1:p.Glu2380=
XM_017009766.1:c.4970A= XP_016865255.1:p.Glu1657=
XM_024446183.1:c.8138A= XP_024301951.1:p.Glu2713=
XM_024446184.1:c.8009A= XP_024301952.1:p.Glu2670=
XM_024446185.1:c.7655A= XP_024301953.1:p.Glu2552=
XM_024446186.1:c.7334A= XP_024301954.1:p.Glu2445=
XR_001742208.1:n.8496A=
XR_002956171.1:n.8442A=
XR_925644.2:n.8551A=
NM_001384732.1:c.8327A= MANE Select NP_001371661.1:p.Glu2776=
NM_023073.4:c.8165A= NP_075561.3:p.Glu2722=