Canonical Allele Identifier: CA2739880862

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37157366A>G , CM000667.2:g.37157366A>G	GRCh38
NC_000005.9:g.37157468A>G , CM000667.1:g.37157468A>G	GRCh37
NC_000005.8:g.37193225A>G	NCBI36
NG_032772.1:g.97063T>C
NG_032772.2:g.97063T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1065T>C
ENST00000651892.2:c.8066T>C MANE Select	ENSP00000498265.2:p.Val2689Ala
ENST00000425232.6:c.7957+304T>C	ENSP00000389014.2:n.7957+304T>C
ENST00000508244.5:c.7957+304T>C	ENSP00000421690.1:n.7957+304T>C
ENST00000509849.5:c.5078T>C	ENSP00000426337.1:p.Val1693Ala
ENST00000509957.5:n.308T>C
ENST00000511210.5:n.357T>C
ENST00000511824.2:c.1180T>C
ENST00000514429.5:c.5155+304T>C	ENSP00000424223.1:n.5155+304T>C
ENST00000515380.1:n.318T>C
NM_023073.3:c.7957+304T>C	NP_075561.3:n.7957+304T>C
XM_005248345.2:c.8066T>C	XP_005248402.1:p.Val2689Ala
XM_005248346.2:c.8063T>C	XP_005248403.1:p.Val2688Ala
XM_005248347.2:c.8063T>C	XP_005248404.1:p.Val2688Ala
XM_005248349.2:c.8008+304T>C	XP_005248406.1:n.8008+304T>C
XM_005248350.2:c.7937T>C	XP_005248407.1:p.Val2646Ala
XM_005248353.3:c.4709T>C	XP_005248410.1:p.Val1570Ala
XM_006714489.2:c.8066T>C	XP_006714552.1:p.Val2689Ala
XM_006714491.2:c.2639T>C	XP_006714554.1:p.Val880Ala
XM_011514085.1:c.8066T>C	XP_011512387.1:p.Val2689Ala
XM_011514086.1:c.8066T>C	XP_011512388.1:p.Val2689Ala
XM_011514087.1:c.8012T>C	XP_011512389.1:p.Val2671Ala
XM_011514088.1:c.8011+304T>C	XP_011512390.1:n.8011+304T>C
XM_011514089.1:c.8066T>C	XP_011512391.1:p.Val2689Ala
XM_011514090.1:c.7748T>C	XP_011512392.1:p.Val2583Ala
XM_011514091.1:c.7394T>C	XP_011512393.1:p.Val2465Ala
XM_011514092.1:c.8066T>C	XP_011512394.1:p.Val2689Ala
XM_011514094.1:c.5291T>C	XP_011512396.1:p.Val1764Ala
XR_427661.2:n.8241T>C
XR_925644.1:n.8241T>C
XM_005248345.4:c.8066T>C	XP_005248402.1:p.Val2689Ala
XM_005248346.4:c.8063T>C	XP_005248403.1:p.Val2688Ala
XM_005248347.4:c.8063T>C	XP_005248404.1:p.Val2688Ala
XM_005248349.4:c.8008+304T>C	XP_005248406.1:n.8008+304T>C
XM_005248350.4:c.7937T>C	XP_005248407.1:p.Val2646Ala
XM_006714491.3:c.2639T>C	XP_006714554.1:p.Val880Ala
XM_011514085.3:c.8066T>C	XP_011512387.1:p.Val2689Ala
XM_011514086.3:c.8066T>C	XP_011512388.1:p.Val2689Ala
XM_011514087.2:c.8012T>C	XP_011512389.1:p.Val2671Ala
XM_011514088.2:c.8011+304T>C	XP_011512390.1:n.8011+304T>C
XM_011514089.2:c.8066T>C	XP_011512391.1:p.Val2689Ala
XM_011514090.3:c.7748T>C	XP_011512392.1:p.Val2583Ala
XM_011514092.2:c.8066T>C	XP_011512394.1:p.Val2689Ala
XM_011514094.2:c.5291T>C	XP_011512396.1:p.Val1764Ala
XM_017009760.1:c.7877T>C	XP_016865249.1:p.Val2626Ala
XM_017009761.2:c.7877T>C	XP_016865250.1:p.Val2626Ala
XM_017009763.1:c.7073T>C	XP_016865252.1:p.Val2358Ala
XM_017009765.1:c.6878T>C	XP_016865254.1:p.Val2293Ala
XM_017009766.1:c.4709T>C	XP_016865255.1:p.Val1570Ala
XM_024446183.1:c.7877T>C	XP_024301951.1:p.Val2626Ala
XM_024446184.1:c.7748T>C	XP_024301952.1:p.Val2583Ala
XM_024446185.1:c.7394T>C	XP_024301953.1:p.Val2465Ala
XM_024446186.1:c.7073T>C	XP_024301954.1:p.Val2358Ala
XR_001742208.1:n.8235T>C
XR_002956171.1:n.8181T>C
XR_925644.2:n.8290T>C
NM_001384732.1:c.8066T>C MANE Select	NP_001371661.1:p.Val2689Ala
NM_023073.4:c.7957+304T>C	NP_075561.3:n.7957+304T>C