Canonical Allele Identifier: CA359474341

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154066C>A (hg19) ; chr5:g.37153964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153964C>A , CM000667.2:g.37153964C>A	GRCh38
NC_000005.9:g.37154066C>A , CM000667.1:g.37154066C>A	GRCh37
NC_000005.8:g.37189823C>A	NCBI36
NG_032772.1:g.100465G>T
NG_032772.2:g.100465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1148G>T
ENST00000651892.2:c.8149G>T MANE Select	ENSP00000498265.2:p.Gly2717Ter
ENST00000425232.6:c.7987G>T	ENSP00000389014.2:p.Gly2663Ter
ENST00000508244.5:c.7987G>T	ENSP00000421690.1:p.Gly2663Ter
ENST00000509849.5:c.5161G>T	ENSP00000426337.1:p.Gly1721Ter
ENST00000509957.5:n.391G>T
ENST00000511210.5:n.440G>T
ENST00000511824.2:c.1263G>T
ENST00000514429.5:c.5185G>T	ENSP00000424223.1:p.Gly1729Ter
ENST00000515380.1:n.401G>T
NM_023073.3:c.7987G>T	NP_075561.3:p.Gly2663Ter
XM_005248345.2:c.8149G>T	XP_005248402.1:p.Gly2717Ter
XM_005248346.2:c.8146G>T	XP_005248403.1:p.Gly2716Ter
XM_005248347.2:c.8146G>T	XP_005248404.1:p.Gly2716Ter
XM_005248349.2:c.8038G>T	XP_005248406.1:p.Gly2680Ter
XM_005248350.2:c.8020G>T	XP_005248407.1:p.Gly2674Ter
XM_005248353.3:c.4792G>T	XP_005248410.1:p.Gly1598Ter
XM_006714489.2:c.8149G>T	XP_006714552.1:p.Gly2717Ter
XM_006714491.2:c.2722G>T	XP_006714554.1:p.Gly908Ter
XM_011514085.1:c.8149G>T	XP_011512387.1:p.Gly2717Ter
XM_011514086.1:c.8149G>T	XP_011512388.1:p.Gly2717Ter
XM_011514087.1:c.8095G>T	XP_011512389.1:p.Gly2699Ter
XM_011514088.1:c.8041G>T	XP_011512390.1:p.Gly2681Ter
XM_011514089.1:c.8149G>T	XP_011512391.1:p.Gly2717Ter
XM_011514090.1:c.7831G>T	XP_011512392.1:p.Gly2611Ter
XM_011514091.1:c.7477G>T	XP_011512393.1:p.Gly2493Ter
XM_011514092.1:c.8149G>T	XP_011512394.1:p.Gly2717Ter
XM_011514094.1:c.5374G>T	XP_011512396.1:p.Gly1792Ter
XR_427661.2:n.8324G>T
XR_925644.1:n.8324G>T
XM_005248345.4:c.8149G>T	XP_005248402.1:p.Gly2717Ter
XM_005248346.4:c.8146G>T	XP_005248403.1:p.Gly2716Ter
XM_005248347.4:c.8146G>T	XP_005248404.1:p.Gly2716Ter
XM_005248349.4:c.8038G>T	XP_005248406.1:p.Gly2680Ter
XM_005248350.4:c.8020G>T	XP_005248407.1:p.Gly2674Ter
XM_006714491.3:c.2722G>T	XP_006714554.1:p.Gly908Ter
XM_011514085.3:c.8149G>T	XP_011512387.1:p.Gly2717Ter
XM_011514086.3:c.8149G>T	XP_011512388.1:p.Gly2717Ter
XM_011514087.2:c.8095G>T	XP_011512389.1:p.Gly2699Ter
XM_011514088.2:c.8041G>T	XP_011512390.1:p.Gly2681Ter
XM_011514089.2:c.8149G>T	XP_011512391.1:p.Gly2717Ter
XM_011514090.3:c.7831G>T	XP_011512392.1:p.Gly2611Ter
XM_011514092.2:c.8149G>T	XP_011512394.1:p.Gly2717Ter
XM_011514094.2:c.5374G>T	XP_011512396.1:p.Gly1792Ter
XM_017009760.1:c.7960G>T	XP_016865249.1:p.Gly2654Ter
XM_017009761.2:c.7960G>T	XP_016865250.1:p.Gly2654Ter
XM_017009763.1:c.7156G>T	XP_016865252.1:p.Gly2386Ter
XM_017009765.1:c.6961G>T	XP_016865254.1:p.Gly2321Ter
XM_017009766.1:c.4792G>T	XP_016865255.1:p.Gly1598Ter
XM_024446183.1:c.7960G>T	XP_024301951.1:p.Gly2654Ter
XM_024446184.1:c.7831G>T	XP_024301952.1:p.Gly2611Ter
XM_024446185.1:c.7477G>T	XP_024301953.1:p.Gly2493Ter
XM_024446186.1:c.7156G>T	XP_024301954.1:p.Gly2386Ter
XR_001742208.1:n.8318G>T
XR_002956171.1:n.8264G>T
XR_925644.2:n.8373G>T
NM_001384732.1:c.8149G>T MANE Select	NP_001371661.1:p.Gly2717Ter
NM_023073.4:c.7987G>T	NP_075561.3:p.Gly2663Ter