Canonical Allele Identifier: CA1539650967
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37153769G= , CM000667.2:g.37153769G= GRCh38
NC_000005.9:g.37153871G= , CM000667.1:g.37153871G= GRCh37
NC_000005.8:g.37189628G= NCBI36
NG_032772.1:g.100660C=
NG_032772.2:g.100660C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000510830.2:n.1343C=
ENST00000651892.2:c.8344C= MANE Select ENSP00000498265.2:p.Pro2782=
ENST00000425232.6:c.8182C= ENSP00000389014.2:p.Pro2728=
ENST00000508244.5:c.8182C= ENSP00000421690.1:p.Pro2728=
ENST00000508405.1:n.76C=
ENST00000509849.5:c.5356C= ENSP00000426337.1:p.Pro1786=
ENST00000509957.5:n.586C=
ENST00000511824.2:c.1458C=
ENST00000514429.5:c.5380C= ENSP00000424223.1:p.Pro1794=
NM_023073.3:c.8182C= NP_075561.3:p.Pro2728=
XM_005248345.2:c.8344C= XP_005248402.1:p.Pro2782=
XM_005248346.2:c.8341C= XP_005248403.1:p.Pro2781=
XM_005248347.2:c.8341C= XP_005248404.1:p.Pro2781=
XM_005248349.2:c.8233C= XP_005248406.1:p.Pro2745=
XM_005248350.2:c.8215C= XP_005248407.1:p.Pro2739=
XM_005248353.3:c.4987C= XP_005248410.1:p.Pro1663=
XM_006714489.2:c.8344C= XP_006714552.1:p.Pro2782=
XM_006714491.2:c.2917C= XP_006714554.1:p.Pro973=
XM_011514085.1:c.8344C= XP_011512387.1:p.Pro2782=
XM_011514086.1:c.8344C= XP_011512388.1:p.Pro2782=
XM_011514087.1:c.8290C= XP_011512389.1:p.Pro2764=
XM_011514088.1:c.8236C= XP_011512390.1:p.Pro2746=
XM_011514089.1:c.8344C= XP_011512391.1:p.Pro2782=
XM_011514090.1:c.8026C= XP_011512392.1:p.Pro2676=
XM_011514091.1:c.7672C= XP_011512393.1:p.Pro2558=
XM_011514092.1:c.8344C= XP_011512394.1:p.Pro2782=
XM_011514094.1:c.5569C= XP_011512396.1:p.Pro1857=
XR_427661.2:n.8519C=
XR_925644.1:n.8519C=
XM_005248345.4:c.8344C= XP_005248402.1:p.Pro2782=
XM_005248346.4:c.8341C= XP_005248403.1:p.Pro2781=
XM_005248347.4:c.8341C= XP_005248404.1:p.Pro2781=
XM_005248349.4:c.8233C= XP_005248406.1:p.Pro2745=
XM_005248350.4:c.8215C= XP_005248407.1:p.Pro2739=
XM_006714491.3:c.2917C= XP_006714554.1:p.Pro973=
XM_011514085.3:c.8344C= XP_011512387.1:p.Pro2782=
XM_011514086.3:c.8344C= XP_011512388.1:p.Pro2782=
XM_011514087.2:c.8290C= XP_011512389.1:p.Pro2764=
XM_011514088.2:c.8236C= XP_011512390.1:p.Pro2746=
XM_011514089.2:c.8344C= XP_011512391.1:p.Pro2782=
XM_011514090.3:c.8026C= XP_011512392.1:p.Pro2676=
XM_011514092.2:c.8344C= XP_011512394.1:p.Pro2782=
XM_011514094.2:c.5569C= XP_011512396.1:p.Pro1857=
XM_017009760.1:c.8155C= XP_016865249.1:p.Pro2719=
XM_017009761.2:c.8155C= XP_016865250.1:p.Pro2719=
XM_017009763.1:c.7351C= XP_016865252.1:p.Pro2451=
XM_017009765.1:c.7156C= XP_016865254.1:p.Pro2386=
XM_017009766.1:c.4987C= XP_016865255.1:p.Pro1663=
XM_024446183.1:c.8155C= XP_024301951.1:p.Pro2719=
XM_024446184.1:c.8026C= XP_024301952.1:p.Pro2676=
XM_024446185.1:c.7672C= XP_024301953.1:p.Pro2558=
XM_024446186.1:c.7351C= XP_024301954.1:p.Pro2451=
XR_001742208.1:n.8513C=
XR_002956171.1:n.8459C=
XR_925644.2:n.8568C=
NM_001384732.1:c.8344C= MANE Select NP_001371661.1:p.Pro2782=
NM_023073.4:c.8182C= NP_075561.3:p.Pro2728=