Canonical Allele Identifier: CA359474059

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37153988C>A (hg19) ; chr5:g.37153886C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153886C>A , CM000667.2:g.37153886C>A	GRCh38
NC_000005.9:g.37153988C>A , CM000667.1:g.37153988C>A	GRCh37
NC_000005.8:g.37189745C>A	NCBI36
NG_032772.1:g.100543G>T
NG_032772.2:g.100543G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1226G>T
ENST00000651892.2:c.8227G>T MANE Select	ENSP00000498265.2:p.Ala2743Ser
ENST00000425232.6:c.8065G>T	ENSP00000389014.2:p.Ala2689Ser
ENST00000508244.5:c.8065G>T	ENSP00000421690.1:p.Ala2689Ser
ENST00000509849.5:c.5239G>T	ENSP00000426337.1:p.Ala1747Ser
ENST00000509957.5:n.469G>T
ENST00000511210.5:n.518G>T
ENST00000511824.2:c.1341G>T
ENST00000514429.5:c.5263G>T	ENSP00000424223.1:p.Ala1755Ser
NM_023073.3:c.8065G>T	NP_075561.3:p.Ala2689Ser
XM_005248345.2:c.8227G>T	XP_005248402.1:p.Ala2743Ser
XM_005248346.2:c.8224G>T	XP_005248403.1:p.Ala2742Ser
XM_005248347.2:c.8224G>T	XP_005248404.1:p.Ala2742Ser
XM_005248349.2:c.8116G>T	XP_005248406.1:p.Ala2706Ser
XM_005248350.2:c.8098G>T	XP_005248407.1:p.Ala2700Ser
XM_005248353.3:c.4870G>T	XP_005248410.1:p.Ala1624Ser
XM_006714489.2:c.8227G>T	XP_006714552.1:p.Ala2743Ser
XM_006714491.2:c.2800G>T	XP_006714554.1:p.Ala934Ser
XM_011514085.1:c.8227G>T	XP_011512387.1:p.Ala2743Ser
XM_011514086.1:c.8227G>T	XP_011512388.1:p.Ala2743Ser
XM_011514087.1:c.8173G>T	XP_011512389.1:p.Ala2725Ser
XM_011514088.1:c.8119G>T	XP_011512390.1:p.Ala2707Ser
XM_011514089.1:c.8227G>T	XP_011512391.1:p.Ala2743Ser
XM_011514090.1:c.7909G>T	XP_011512392.1:p.Ala2637Ser
XM_011514091.1:c.7555G>T	XP_011512393.1:p.Ala2519Ser
XM_011514092.1:c.8227G>T	XP_011512394.1:p.Ala2743Ser
XM_011514094.1:c.5452G>T	XP_011512396.1:p.Ala1818Ser
XR_427661.2:n.8402G>T
XR_925644.1:n.8402G>T
XM_005248345.4:c.8227G>T	XP_005248402.1:p.Ala2743Ser
XM_005248346.4:c.8224G>T	XP_005248403.1:p.Ala2742Ser
XM_005248347.4:c.8224G>T	XP_005248404.1:p.Ala2742Ser
XM_005248349.4:c.8116G>T	XP_005248406.1:p.Ala2706Ser
XM_005248350.4:c.8098G>T	XP_005248407.1:p.Ala2700Ser
XM_006714491.3:c.2800G>T	XP_006714554.1:p.Ala934Ser
XM_011514085.3:c.8227G>T	XP_011512387.1:p.Ala2743Ser
XM_011514086.3:c.8227G>T	XP_011512388.1:p.Ala2743Ser
XM_011514087.2:c.8173G>T	XP_011512389.1:p.Ala2725Ser
XM_011514088.2:c.8119G>T	XP_011512390.1:p.Ala2707Ser
XM_011514089.2:c.8227G>T	XP_011512391.1:p.Ala2743Ser
XM_011514090.3:c.7909G>T	XP_011512392.1:p.Ala2637Ser
XM_011514092.2:c.8227G>T	XP_011512394.1:p.Ala2743Ser
XM_011514094.2:c.5452G>T	XP_011512396.1:p.Ala1818Ser
XM_017009760.1:c.8038G>T	XP_016865249.1:p.Ala2680Ser
XM_017009761.2:c.8038G>T	XP_016865250.1:p.Ala2680Ser
XM_017009763.1:c.7234G>T	XP_016865252.1:p.Ala2412Ser
XM_017009765.1:c.7039G>T	XP_016865254.1:p.Ala2347Ser
XM_017009766.1:c.4870G>T	XP_016865255.1:p.Ala1624Ser
XM_024446183.1:c.8038G>T	XP_024301951.1:p.Ala2680Ser
XM_024446184.1:c.7909G>T	XP_024301952.1:p.Ala2637Ser
XM_024446185.1:c.7555G>T	XP_024301953.1:p.Ala2519Ser
XM_024446186.1:c.7234G>T	XP_024301954.1:p.Ala2412Ser
XR_001742208.1:n.8396G>T
XR_002956171.1:n.8342G>T
XR_925644.2:n.8451G>T
NM_001384732.1:c.8227G>T MANE Select	NP_001371661.1:p.Ala2743Ser
NM_023073.4:c.8065G>T	NP_075561.3:p.Ala2689Ser