Canonical Allele Identifier: CA1539651096
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37153822T= , CM000667.2:g.37153822T= GRCh38
NC_000005.9:g.37153924T= , CM000667.1:g.37153924T= GRCh37
NC_000005.8:g.37189681T= NCBI36
NG_032772.1:g.100607A=
NG_032772.2:g.100607A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1290A=
ENST00000651892.2:c.8291A= MANE Select ENSP00000498265.2:p.Gln2764=
ENST00000425232.6:c.8129A= ENSP00000389014.2:p.Gln2710=
ENST00000508244.5:c.8129A= ENSP00000421690.1:p.Gln2710=
ENST00000508405.1:n.23A=
ENST00000509849.5:c.5303A= ENSP00000426337.1:p.Gln1768=
ENST00000509957.5:n.533A=
ENST00000511824.2:c.1405A=
ENST00000514429.5:c.5327A= ENSP00000424223.1:p.Gln1776=
NM_023073.3:c.8129A= NP_075561.3:p.Gln2710=
XM_005248345.2:c.8291A= XP_005248402.1:p.Gln2764=
XM_005248346.2:c.8288A= XP_005248403.1:p.Gln2763=
XM_005248347.2:c.8288A= XP_005248404.1:p.Gln2763=
XM_005248349.2:c.8180A= XP_005248406.1:p.Gln2727=
XM_005248350.2:c.8162A= XP_005248407.1:p.Gln2721=
XM_005248353.3:c.4934A= XP_005248410.1:p.Gln1645=
XM_006714489.2:c.8291A= XP_006714552.1:p.Gln2764=
XM_006714491.2:c.2864A= XP_006714554.1:p.Gln955=
XM_011514085.1:c.8291A= XP_011512387.1:p.Gln2764=
XM_011514086.1:c.8291A= XP_011512388.1:p.Gln2764=
XM_011514087.1:c.8237A= XP_011512389.1:p.Gln2746=
XM_011514088.1:c.8183A= XP_011512390.1:p.Gln2728=
XM_011514089.1:c.8291A= XP_011512391.1:p.Gln2764=
XM_011514090.1:c.7973A= XP_011512392.1:p.Gln2658=
XM_011514091.1:c.7619A= XP_011512393.1:p.Gln2540=
XM_011514092.1:c.8291A= XP_011512394.1:p.Gln2764=
XM_011514094.1:c.5516A= XP_011512396.1:p.Gln1839=
XR_427661.2:n.8466A=
XR_925644.1:n.8466A=
XM_005248345.4:c.8291A= XP_005248402.1:p.Gln2764=
XM_005248346.4:c.8288A= XP_005248403.1:p.Gln2763=
XM_005248347.4:c.8288A= XP_005248404.1:p.Gln2763=
XM_005248349.4:c.8180A= XP_005248406.1:p.Gln2727=
XM_005248350.4:c.8162A= XP_005248407.1:p.Gln2721=
XM_006714491.3:c.2864A= XP_006714554.1:p.Gln955=
XM_011514085.3:c.8291A= XP_011512387.1:p.Gln2764=
XM_011514086.3:c.8291A= XP_011512388.1:p.Gln2764=
XM_011514087.2:c.8237A= XP_011512389.1:p.Gln2746=
XM_011514088.2:c.8183A= XP_011512390.1:p.Gln2728=
XM_011514089.2:c.8291A= XP_011512391.1:p.Gln2764=
XM_011514090.3:c.7973A= XP_011512392.1:p.Gln2658=
XM_011514092.2:c.8291A= XP_011512394.1:p.Gln2764=
XM_011514094.2:c.5516A= XP_011512396.1:p.Gln1839=
XM_017009760.1:c.8102A= XP_016865249.1:p.Gln2701=
XM_017009761.2:c.8102A= XP_016865250.1:p.Gln2701=
XM_017009763.1:c.7298A= XP_016865252.1:p.Gln2433=
XM_017009765.1:c.7103A= XP_016865254.1:p.Gln2368=
XM_017009766.1:c.4934A= XP_016865255.1:p.Gln1645=
XM_024446183.1:c.8102A= XP_024301951.1:p.Gln2701=
XM_024446184.1:c.7973A= XP_024301952.1:p.Gln2658=
XM_024446185.1:c.7619A= XP_024301953.1:p.Gln2540=
XM_024446186.1:c.7298A= XP_024301954.1:p.Gln2433=
XR_001742208.1:n.8460A=
XR_002956171.1:n.8406A=
XR_925644.2:n.8515A=
NM_001384732.1:c.8291A= MANE Select NP_001371661.1:p.Gln2764=
NM_023073.4:c.8129A= NP_075561.3:p.Gln2710=