Canonical Allele Identifier: CA2739880819

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37157339G>A , CM000667.2:g.37157339G>A	GRCh38
NC_000005.9:g.37157441G>A , CM000667.1:g.37157441G>A	GRCh37
NC_000005.8:g.37193198G>A	NCBI36
NG_032772.1:g.97090C>T
NG_032772.2:g.97090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1092C>T
ENST00000651892.2:c.8093C>T MANE Select	ENSP00000498265.2:p.Thr2698Ile
ENST00000425232.6:c.7957+331C>T	ENSP00000389014.2:n.7957+331C>T
ENST00000508244.5:c.7957+331C>T	ENSP00000421690.1:n.7957+331C>T
ENST00000509849.5:c.5105C>T	ENSP00000426337.1:p.Thr1702Ile
ENST00000509957.5:n.335C>T
ENST00000511210.5:n.384C>T
ENST00000511824.2:c.1207C>T
ENST00000514429.5:c.5155+331C>T	ENSP00000424223.1:n.5155+331C>T
ENST00000515380.1:n.345C>T
NM_023073.3:c.7957+331C>T	NP_075561.3:n.7957+331C>T
XM_005248345.2:c.8093C>T	XP_005248402.1:p.Thr2698Ile
XM_005248346.2:c.8090C>T	XP_005248403.1:p.Thr2697Ile
XM_005248347.2:c.8090C>T	XP_005248404.1:p.Thr2697Ile
XM_005248349.2:c.8008+331C>T	XP_005248406.1:n.8008+331C>T
XM_005248350.2:c.7964C>T	XP_005248407.1:p.Thr2655Ile
XM_005248353.3:c.4736C>T	XP_005248410.1:p.Thr1579Ile
XM_006714489.2:c.8093C>T	XP_006714552.1:p.Thr2698Ile
XM_006714491.2:c.2666C>T	XP_006714554.1:p.Thr889Ile
XM_011514085.1:c.8093C>T	XP_011512387.1:p.Thr2698Ile
XM_011514086.1:c.8093C>T	XP_011512388.1:p.Thr2698Ile
XM_011514087.1:c.8039C>T	XP_011512389.1:p.Thr2680Ile
XM_011514088.1:c.8011+331C>T	XP_011512390.1:n.8011+331C>T
XM_011514089.1:c.8093C>T	XP_011512391.1:p.Thr2698Ile
XM_011514090.1:c.7775C>T	XP_011512392.1:p.Thr2592Ile
XM_011514091.1:c.7421C>T	XP_011512393.1:p.Thr2474Ile
XM_011514092.1:c.8093C>T	XP_011512394.1:p.Thr2698Ile
XM_011514094.1:c.5318C>T	XP_011512396.1:p.Thr1773Ile
XR_427661.2:n.8268C>T
XR_925644.1:n.8268C>T
XM_005248345.4:c.8093C>T	XP_005248402.1:p.Thr2698Ile
XM_005248346.4:c.8090C>T	XP_005248403.1:p.Thr2697Ile
XM_005248347.4:c.8090C>T	XP_005248404.1:p.Thr2697Ile
XM_005248349.4:c.8008+331C>T	XP_005248406.1:n.8008+331C>T
XM_005248350.4:c.7964C>T	XP_005248407.1:p.Thr2655Ile
XM_006714491.3:c.2666C>T	XP_006714554.1:p.Thr889Ile
XM_011514085.3:c.8093C>T	XP_011512387.1:p.Thr2698Ile
XM_011514086.3:c.8093C>T	XP_011512388.1:p.Thr2698Ile
XM_011514087.2:c.8039C>T	XP_011512389.1:p.Thr2680Ile
XM_011514088.2:c.8011+331C>T	XP_011512390.1:n.8011+331C>T
XM_011514089.2:c.8093C>T	XP_011512391.1:p.Thr2698Ile
XM_011514090.3:c.7775C>T	XP_011512392.1:p.Thr2592Ile
XM_011514092.2:c.8093C>T	XP_011512394.1:p.Thr2698Ile
XM_011514094.2:c.5318C>T	XP_011512396.1:p.Thr1773Ile
XM_017009760.1:c.7904C>T	XP_016865249.1:p.Thr2635Ile
XM_017009761.2:c.7904C>T	XP_016865250.1:p.Thr2635Ile
XM_017009763.1:c.7100C>T	XP_016865252.1:p.Thr2367Ile
XM_017009765.1:c.6905C>T	XP_016865254.1:p.Thr2302Ile
XM_017009766.1:c.4736C>T	XP_016865255.1:p.Thr1579Ile
XM_024446183.1:c.7904C>T	XP_024301951.1:p.Thr2635Ile
XM_024446184.1:c.7775C>T	XP_024301952.1:p.Thr2592Ile
XM_024446185.1:c.7421C>T	XP_024301953.1:p.Thr2474Ile
XM_024446186.1:c.7100C>T	XP_024301954.1:p.Thr2367Ile
XR_001742208.1:n.8262C>T
XR_002956171.1:n.8208C>T
XR_925644.2:n.8317C>T
NM_001384732.1:c.8093C>T MANE Select	NP_001371661.1:p.Thr2698Ile
NM_023073.4:c.7957+331C>T	NP_075561.3:n.7957+331C>T