Canonical Allele Identifier: CA444096496

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154094A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153992A>T , CM000667.2:g.37153992A>T	GRCh38
NC_000005.9:g.37154094A>T , CM000667.1:g.37154094A>T	GRCh37
NC_000005.8:g.37189851A>T	NCBI36
NG_032772.1:g.100437T>A
NG_032772.2:g.100437T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1120T>A
ENST00000651892.2:c.8121T>A MANE Select	ENSP00000498265.2:p.Gly2707=
ENST00000425232.6:c.7959T>A	ENSP00000389014.2:p.Gly2653=
ENST00000508244.5:c.7959T>A	ENSP00000421690.1:p.Gly2653=
ENST00000509849.5:c.5133T>A	ENSP00000426337.1:p.Gly1711=
ENST00000509957.5:n.363T>A
ENST00000511210.5:n.412T>A
ENST00000511824.2:c.1235T>A
ENST00000514429.5:c.5157T>A	ENSP00000424223.1:p.Gly1719=
ENST00000515380.1:n.373T>A
NM_023073.3:c.7959T>A	NP_075561.3:p.Gly2653=
XM_005248345.2:c.8121T>A	XP_005248402.1:p.Gly2707=
XM_005248346.2:c.8118T>A	XP_005248403.1:p.Gly2706=
XM_005248347.2:c.8118T>A	XP_005248404.1:p.Gly2706=
XM_005248349.2:c.8010T>A	XP_005248406.1:p.Gly2670=
XM_005248350.2:c.7992T>A	XP_005248407.1:p.Gly2664=
XM_005248353.3:c.4764T>A	XP_005248410.1:p.Gly1588=
XM_006714489.2:c.8121T>A	XP_006714552.1:p.Gly2707=
XM_006714491.2:c.2694T>A	XP_006714554.1:p.Gly898=
XM_011514085.1:c.8121T>A	XP_011512387.1:p.Gly2707=
XM_011514086.1:c.8121T>A	XP_011512388.1:p.Gly2707=
XM_011514087.1:c.8067T>A	XP_011512389.1:p.Gly2689=
XM_011514088.1:c.8013T>A	XP_011512390.1:p.Gly2671=
XM_011514089.1:c.8121T>A	XP_011512391.1:p.Gly2707=
XM_011514090.1:c.7803T>A	XP_011512392.1:p.Gly2601=
XM_011514091.1:c.7449T>A	XP_011512393.1:p.Gly2483=
XM_011514092.1:c.8121T>A	XP_011512394.1:p.Gly2707=
XM_011514094.1:c.5346T>A	XP_011512396.1:p.Gly1782=
XR_427661.2:n.8296T>A
XR_925644.1:n.8296T>A
XM_005248345.4:c.8121T>A	XP_005248402.1:p.Gly2707=
XM_005248346.4:c.8118T>A	XP_005248403.1:p.Gly2706=
XM_005248347.4:c.8118T>A	XP_005248404.1:p.Gly2706=
XM_005248349.4:c.8010T>A	XP_005248406.1:p.Gly2670=
XM_005248350.4:c.7992T>A	XP_005248407.1:p.Gly2664=
XM_006714491.3:c.2694T>A	XP_006714554.1:p.Gly898=
XM_011514085.3:c.8121T>A	XP_011512387.1:p.Gly2707=
XM_011514086.3:c.8121T>A	XP_011512388.1:p.Gly2707=
XM_011514087.2:c.8067T>A	XP_011512389.1:p.Gly2689=
XM_011514088.2:c.8013T>A	XP_011512390.1:p.Gly2671=
XM_011514089.2:c.8121T>A	XP_011512391.1:p.Gly2707=
XM_011514090.3:c.7803T>A	XP_011512392.1:p.Gly2601=
XM_011514092.2:c.8121T>A	XP_011512394.1:p.Gly2707=
XM_011514094.2:c.5346T>A	XP_011512396.1:p.Gly1782=
XM_017009760.1:c.7932T>A	XP_016865249.1:p.Gly2644=
XM_017009761.2:c.7932T>A	XP_016865250.1:p.Gly2644=
XM_017009763.1:c.7128T>A	XP_016865252.1:p.Gly2376=
XM_017009765.1:c.6933T>A	XP_016865254.1:p.Gly2311=
XM_017009766.1:c.4764T>A	XP_016865255.1:p.Gly1588=
XM_024446183.1:c.7932T>A	XP_024301951.1:p.Gly2644=
XM_024446184.1:c.7803T>A	XP_024301952.1:p.Gly2601=
XM_024446185.1:c.7449T>A	XP_024301953.1:p.Gly2483=
XM_024446186.1:c.7128T>A	XP_024301954.1:p.Gly2376=
XR_001742208.1:n.8290T>A
XR_002956171.1:n.8236T>A
XR_925644.2:n.8345T>A
NM_001384732.1:c.8121T>A MANE Select	NP_001371661.1:p.Gly2707=
NM_023073.4:c.7959T>A	NP_075561.3:p.Gly2653=