Canonical Allele Identifier: CA3237637
Community Standard Title: NM_001384732.1(CPLANE1):c.8873G>A (p.Arg2958Gln)
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37125329C>T , CM000667.2:g.37125329C>T GRCh38
NC_000005.9:g.37125431C>T , CM000667.1:g.37125431C>T GRCh37
NC_000005.8:g.37161188C>T NCBI36
NG_032772.1:g.129100G>A
NG_032772.2:g.129100G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001384732.1:c.8873G>A MANE Select NP_001371661.1:p.Arg2958Gln
ENST00000651892.2:c.8873G>A MANE Select ENSP00000498265.2:p.Arg2958Gln
NM_023073.3:c.8711G>A NP_075561.3:p.Arg2904Gln
NM_023073.4:c.8711G>A NP_075561.3:p.Arg2904Gln
ENST00000425232.6:c.8711G>A ENSP00000389014.2:p.Arg2904Gln
ENST00000508244.5:c.8711G>A ENSP00000421690.1:p.Arg2904Gln
ENST00000509849.5:c.5885G>A ENSP00000426337.1:n.5885G>A
ENST00000509957.5:n.4054G>A
ENST00000510830.2:n.1872G>A
ENST00000512288.5:n.342-3545G>A
ENST00000514429.5:c.5909G>A ENSP00000424223.1:p.Arg1970Gln
ENST00000676160.1:n.734G>A
XM_005248345.2:c.8873G>A XP_005248402.1:p.Arg2958Gln
XM_005248345.4:c.8873G>A XP_005248402.1:p.Arg2958Gln
XM_005248346.2:c.8870G>A XP_005248403.1:p.Arg2957Gln
XM_005248346.4:c.8870G>A XP_005248403.1:p.Arg2957Gln
XM_005248347.2:c.8870G>A XP_005248404.1:p.Arg2957Gln
XM_005248347.4:c.8870G>A XP_005248404.1:p.Arg2957Gln
XM_005248349.2:c.8762G>A XP_005248406.1:p.Arg2921Gln
XM_005248349.4:c.8762G>A XP_005248406.1:p.Arg2921Gln
XM_005248350.2:c.8744G>A XP_005248407.1:p.Arg2915Gln
XM_005248350.4:c.8744G>A XP_005248407.1:p.Arg2915Gln
XM_005248353.3:c.5516G>A XP_005248410.1:p.Arg1839Gln
XM_006714489.2:c.8873G>A XP_006714552.1:p.Arg2958Gln
XM_006714491.2:c.3446G>A XP_006714554.1:p.Arg1149Gln
XM_006714491.3:c.3446G>A XP_006714554.1:p.Arg1149Gln
XM_011514085.1:c.8873G>A XP_011512387.1:p.Arg2958Gln
XM_011514085.3:c.8873G>A XP_011512387.1:p.Arg2958Gln
XM_011514086.1:c.8873G>A XP_011512388.1:p.Arg2958Gln
XM_011514086.3:c.8873G>A XP_011512388.1:p.Arg2958Gln
XM_011514087.1:c.8819G>A XP_011512389.1:p.Arg2940Gln
XM_011514087.2:c.8819G>A XP_011512389.1:p.Arg2940Gln
XM_011514088.1:c.8765G>A XP_011512390.1:p.Arg2922Gln
XM_011514088.2:c.8765G>A XP_011512390.1:p.Arg2922Gln
XM_011514089.1:c.8873G>A XP_011512391.1:p.Arg2958Gln
XM_011514089.2:c.8873G>A XP_011512391.1:p.Arg2958Gln
XM_011514090.1:c.8555G>A XP_011512392.1:p.Arg2852Gln
XM_011514090.3:c.8555G>A XP_011512392.1:p.Arg2852Gln
XM_011514091.1:c.8201G>A XP_011512393.1:p.Arg2734Gln
XM_011514092.1:c.8873G>A XP_011512394.1:p.Arg2958Gln
XM_011514092.2:c.8873G>A XP_011512394.1:p.Arg2958Gln
XM_011514094.1:c.6098G>A XP_011512396.1:p.Arg2033Gln
XM_011514094.2:c.6098G>A XP_011512396.1:p.Arg2033Gln
XM_017009760.1:c.8684G>A XP_016865249.1:p.Arg2895Gln
XM_017009761.2:c.8684G>A XP_016865250.1:p.Arg2895Gln
XM_017009763.1:c.7880G>A XP_016865252.1:p.Arg2627Gln
XM_017009765.1:c.7685G>A XP_016865254.1:p.Arg2562Gln
XM_017009766.1:c.5516G>A XP_016865255.1:p.Arg1839Gln
XM_024446183.1:c.8684G>A XP_024301951.1:p.Arg2895Gln
XM_024446184.1:c.8555G>A XP_024301952.1:p.Arg2852Gln
XM_024446185.1:c.8201G>A XP_024301953.1:p.Arg2734Gln
XM_024446186.1:c.7880G>A XP_024301954.1:p.Arg2627Gln
XR_427661.2:n.9048G>A
XR_925644.1:n.9048G>A
XR_925644.2:n.9097G>A