Canonical Allele Identifier: CA1539667624
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37125297G= , CM000667.2:g.37125297G= GRCh38
NC_000005.9:g.37125399G= , CM000667.1:g.37125399G= GRCh37
NC_000005.8:g.37161156G= NCBI36
NG_032772.1:g.129132C=
NG_032772.2:g.129132C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1904C=
ENST00000651892.2:c.8905C= MANE Select ENSP00000498265.2:p.Leu2969=
ENST00000676160.1:n.766C=
ENST00000425232.6:c.8743C= ENSP00000389014.2:p.Leu2915=
ENST00000508244.5:c.8743C= ENSP00000421690.1:p.Leu2915=
ENST00000509849.5:c.5917C= ENSP00000426337.1:n.5917C=
ENST00000509957.5:n.4086C=
ENST00000512288.5:n.342-3513C=
ENST00000514429.5:c.5941C= ENSP00000424223.1:p.Leu1981=
NM_023073.3:c.8743C= NP_075561.3:p.Leu2915=
XM_005248345.2:c.8905C= XP_005248402.1:p.Leu2969=
XM_005248346.2:c.8902C= XP_005248403.1:p.Leu2968=
XM_005248347.2:c.8902C= XP_005248404.1:p.Leu2968=
XM_005248349.2:c.8794C= XP_005248406.1:p.Leu2932=
XM_005248350.2:c.8776C= XP_005248407.1:p.Leu2926=
XM_005248353.3:c.5548C= XP_005248410.1:p.Leu1850=
XM_006714489.2:c.8905C= XP_006714552.1:p.Leu2969=
XM_006714491.2:c.3478C= XP_006714554.1:p.Leu1160=
XM_011514085.1:c.8905C= XP_011512387.1:p.Leu2969=
XM_011514086.1:c.8905C= XP_011512388.1:p.Leu2969=
XM_011514087.1:c.8851C= XP_011512389.1:p.Leu2951=
XM_011514088.1:c.8797C= XP_011512390.1:p.Leu2933=
XM_011514089.1:c.8905C= XP_011512391.1:p.Leu2969=
XM_011514090.1:c.8587C= XP_011512392.1:p.Leu2863=
XM_011514091.1:c.8233C= XP_011512393.1:p.Leu2745=
XM_011514092.1:c.8905C= XP_011512394.1:p.Leu2969=
XM_011514094.1:c.6130C= XP_011512396.1:p.Leu2044=
XR_427661.2:n.9080C=
XR_925644.1:n.9080C=
XM_005248345.4:c.8905C= XP_005248402.1:p.Leu2969=
XM_005248346.4:c.8902C= XP_005248403.1:p.Leu2968=
XM_005248347.4:c.8902C= XP_005248404.1:p.Leu2968=
XM_005248349.4:c.8794C= XP_005248406.1:p.Leu2932=
XM_005248350.4:c.8776C= XP_005248407.1:p.Leu2926=
XM_006714491.3:c.3478C= XP_006714554.1:p.Leu1160=
XM_011514085.3:c.8905C= XP_011512387.1:p.Leu2969=
XM_011514086.3:c.8905C= XP_011512388.1:p.Leu2969=
XM_011514087.2:c.8851C= XP_011512389.1:p.Leu2951=
XM_011514088.2:c.8797C= XP_011512390.1:p.Leu2933=
XM_011514089.2:c.8905C= XP_011512391.1:p.Leu2969=
XM_011514090.3:c.8587C= XP_011512392.1:p.Leu2863=
XM_011514092.2:c.8905C= XP_011512394.1:p.Leu2969=
XM_011514094.2:c.6130C= XP_011512396.1:p.Leu2044=
XM_017009760.1:c.8716C= XP_016865249.1:p.Leu2906=
XM_017009761.2:c.8716C= XP_016865250.1:p.Leu2906=
XM_017009763.1:c.7912C= XP_016865252.1:p.Leu2638=
XM_017009765.1:c.7717C= XP_016865254.1:p.Leu2573=
XM_017009766.1:c.5548C= XP_016865255.1:p.Leu1850=
XM_024446183.1:c.8716C= XP_024301951.1:p.Leu2906=
XM_024446184.1:c.8587C= XP_024301952.1:p.Leu2863=
XM_024446185.1:c.8233C= XP_024301953.1:p.Leu2745=
XM_024446186.1:c.7912C= XP_024301954.1:p.Leu2638=
XR_925644.2:n.9129C=
NM_001384732.1:c.8905C= MANE Select NP_001371661.1:p.Leu2969=
NM_023073.4:c.8743C= NP_075561.3:p.Leu2915=