Canonical Allele Identifier: CA1539667747
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37125389C= , CM000667.2:g.37125389C= GRCh38
NC_000005.9:g.37125491C= , CM000667.1:g.37125491C= GRCh37
NC_000005.8:g.37161248C= NCBI36
NG_032772.1:g.129040G=
NG_032772.2:g.129040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1812G=
ENST00000651892.2:c.8813G= MANE Select ENSP00000498265.2:p.Arg2938=
ENST00000676160.1:n.674G=
ENST00000425232.6:c.8651G= ENSP00000389014.2:p.Arg2884=
ENST00000508244.5:c.8651G= ENSP00000421690.1:p.Arg2884=
ENST00000509849.5:c.5825G= ENSP00000426337.1:n.5825G=
ENST00000509957.5:n.3994G=
ENST00000512288.5:n.342-3605G=
ENST00000514429.5:c.5849G= ENSP00000424223.1:p.Arg1950=
NM_023073.3:c.8651G= NP_075561.3:p.Arg2884=
XM_005248345.2:c.8813G= XP_005248402.1:p.Arg2938=
XM_005248346.2:c.8810G= XP_005248403.1:p.Arg2937=
XM_005248347.2:c.8810G= XP_005248404.1:p.Arg2937=
XM_005248349.2:c.8702G= XP_005248406.1:p.Arg2901=
XM_005248350.2:c.8684G= XP_005248407.1:p.Arg2895=
XM_005248353.3:c.5456G= XP_005248410.1:p.Arg1819=
XM_006714489.2:c.8813G= XP_006714552.1:p.Arg2938=
XM_006714491.2:c.3386G= XP_006714554.1:p.Arg1129=
XM_011514085.1:c.8813G= XP_011512387.1:p.Arg2938=
XM_011514086.1:c.8813G= XP_011512388.1:p.Arg2938=
XM_011514087.1:c.8759G= XP_011512389.1:p.Arg2920=
XM_011514088.1:c.8705G= XP_011512390.1:p.Arg2902=
XM_011514089.1:c.8813G= XP_011512391.1:p.Arg2938=
XM_011514090.1:c.8495G= XP_011512392.1:p.Arg2832=
XM_011514091.1:c.8141G= XP_011512393.1:p.Arg2714=
XM_011514092.1:c.8813G= XP_011512394.1:p.Arg2938=
XM_011514094.1:c.6038G= XP_011512396.1:p.Arg2013=
XR_427661.2:n.8988G=
XR_925644.1:n.8988G=
XM_005248345.4:c.8813G= XP_005248402.1:p.Arg2938=
XM_005248346.4:c.8810G= XP_005248403.1:p.Arg2937=
XM_005248347.4:c.8810G= XP_005248404.1:p.Arg2937=
XM_005248349.4:c.8702G= XP_005248406.1:p.Arg2901=
XM_005248350.4:c.8684G= XP_005248407.1:p.Arg2895=
XM_006714491.3:c.3386G= XP_006714554.1:p.Arg1129=
XM_011514085.3:c.8813G= XP_011512387.1:p.Arg2938=
XM_011514086.3:c.8813G= XP_011512388.1:p.Arg2938=
XM_011514087.2:c.8759G= XP_011512389.1:p.Arg2920=
XM_011514088.2:c.8705G= XP_011512390.1:p.Arg2902=
XM_011514089.2:c.8813G= XP_011512391.1:p.Arg2938=
XM_011514090.3:c.8495G= XP_011512392.1:p.Arg2832=
XM_011514092.2:c.8813G= XP_011512394.1:p.Arg2938=
XM_011514094.2:c.6038G= XP_011512396.1:p.Arg2013=
XM_017009760.1:c.8624G= XP_016865249.1:p.Arg2875=
XM_017009761.2:c.8624G= XP_016865250.1:p.Arg2875=
XM_017009763.1:c.7820G= XP_016865252.1:p.Arg2607=
XM_017009765.1:c.7625G= XP_016865254.1:p.Arg2542=
XM_017009766.1:c.5456G= XP_016865255.1:p.Arg1819=
XM_024446183.1:c.8624G= XP_024301951.1:p.Arg2875=
XM_024446184.1:c.8495G= XP_024301952.1:p.Arg2832=
XM_024446185.1:c.8141G= XP_024301953.1:p.Arg2714=
XM_024446186.1:c.7820G= XP_024301954.1:p.Arg2607=
XR_001742208.1:n.8982G=
XR_925644.2:n.9037G=
NM_001384732.1:c.8813G= MANE Select NP_001371661.1:p.Arg2938=
NM_023073.4:c.8651G= NP_075561.3:p.Arg2884=