Canonical Allele Identifier: CA1539667680
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37125351G= , CM000667.2:g.37125351G= GRCh38
NC_000005.9:g.37125453G= , CM000667.1:g.37125453G= GRCh37
NC_000005.8:g.37161210G= NCBI36
NG_032772.1:g.129078C=
NG_032772.2:g.129078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1850C=
ENST00000651892.2:c.8851C= MANE Select ENSP00000498265.2:p.Gln2951=
ENST00000676160.1:n.712C=
ENST00000425232.6:c.8689C= ENSP00000389014.2:p.Gln2897=
ENST00000508244.5:c.8689C= ENSP00000421690.1:p.Gln2897=
ENST00000509849.5:c.5863C= ENSP00000426337.1:n.5863C=
ENST00000509957.5:n.4032C=
ENST00000512288.5:n.342-3567C=
ENST00000514429.5:c.5887C= ENSP00000424223.1:p.Gln1963=
NM_023073.3:c.8689C= NP_075561.3:p.Gln2897=
XM_005248345.2:c.8851C= XP_005248402.1:p.Gln2951=
XM_005248346.2:c.8848C= XP_005248403.1:p.Gln2950=
XM_005248347.2:c.8848C= XP_005248404.1:p.Gln2950=
XM_005248349.2:c.8740C= XP_005248406.1:p.Gln2914=
XM_005248350.2:c.8722C= XP_005248407.1:p.Gln2908=
XM_005248353.3:c.5494C= XP_005248410.1:p.Gln1832=
XM_006714489.2:c.8851C= XP_006714552.1:p.Gln2951=
XM_006714491.2:c.3424C= XP_006714554.1:p.Gln1142=
XM_011514085.1:c.8851C= XP_011512387.1:p.Gln2951=
XM_011514086.1:c.8851C= XP_011512388.1:p.Gln2951=
XM_011514087.1:c.8797C= XP_011512389.1:p.Gln2933=
XM_011514088.1:c.8743C= XP_011512390.1:p.Gln2915=
XM_011514089.1:c.8851C= XP_011512391.1:p.Gln2951=
XM_011514090.1:c.8533C= XP_011512392.1:p.Gln2845=
XM_011514091.1:c.8179C= XP_011512393.1:p.Gln2727=
XM_011514092.1:c.8851C= XP_011512394.1:p.Gln2951=
XM_011514094.1:c.6076C= XP_011512396.1:p.Gln2026=
XR_427661.2:n.9026C=
XR_925644.1:n.9026C=
XM_005248345.4:c.8851C= XP_005248402.1:p.Gln2951=
XM_005248346.4:c.8848C= XP_005248403.1:p.Gln2950=
XM_005248347.4:c.8848C= XP_005248404.1:p.Gln2950=
XM_005248349.4:c.8740C= XP_005248406.1:p.Gln2914=
XM_005248350.4:c.8722C= XP_005248407.1:p.Gln2908=
XM_006714491.3:c.3424C= XP_006714554.1:p.Gln1142=
XM_011514085.3:c.8851C= XP_011512387.1:p.Gln2951=
XM_011514086.3:c.8851C= XP_011512388.1:p.Gln2951=
XM_011514087.2:c.8797C= XP_011512389.1:p.Gln2933=
XM_011514088.2:c.8743C= XP_011512390.1:p.Gln2915=
XM_011514089.2:c.8851C= XP_011512391.1:p.Gln2951=
XM_011514090.3:c.8533C= XP_011512392.1:p.Gln2845=
XM_011514092.2:c.8851C= XP_011512394.1:p.Gln2951=
XM_011514094.2:c.6076C= XP_011512396.1:p.Gln2026=
XM_017009760.1:c.8662C= XP_016865249.1:p.Gln2888=
XM_017009761.2:c.8662C= XP_016865250.1:p.Gln2888=
XM_017009763.1:c.7858C= XP_016865252.1:p.Gln2620=
XM_017009765.1:c.7663C= XP_016865254.1:p.Gln2555=
XM_017009766.1:c.5494C= XP_016865255.1:p.Gln1832=
XM_024446183.1:c.8662C= XP_024301951.1:p.Gln2888=
XM_024446184.1:c.8533C= XP_024301952.1:p.Gln2845=
XM_024446185.1:c.8179C= XP_024301953.1:p.Gln2727=
XM_024446186.1:c.7858C= XP_024301954.1:p.Gln2620=
XR_001742208.1:n.9020C=
XR_925644.2:n.9075C=
NM_001384732.1:c.8851C= MANE Select NP_001371661.1:p.Gln2951=
NM_023073.4:c.8689C= NP_075561.3:p.Gln2897=