Canonical Allele Identifier: CA1539667761

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125401T= , CM000667.2:g.37125401T=	GRCh38
NC_000005.9:g.37125503T= , CM000667.1:g.37125503T=	GRCh37
NC_000005.8:g.37161260T=	NCBI36
NG_032772.1:g.129028A=
NG_032772.2:g.129028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1800A=
ENST00000651892.2:c.8801A= MANE Select	ENSP00000498265.2:p.His2934=
ENST00000676160.1:n.662A=
ENST00000425232.6:c.8639A=	ENSP00000389014.2:p.His2880=
ENST00000508244.5:c.8639A=	ENSP00000421690.1:p.His2880=
ENST00000509849.5:c.5813A=	ENSP00000426337.1:n.5813A=
ENST00000509957.5:n.3982A=
ENST00000512288.5:n.342-3617A=
ENST00000514429.5:c.5837A=	ENSP00000424223.1:p.His1946=
NM_023073.3:c.8639A=	NP_075561.3:p.His2880=
XM_005248345.2:c.8801A=	XP_005248402.1:p.His2934=
XM_005248346.2:c.8798A=	XP_005248403.1:p.His2933=
XM_005248347.2:c.8798A=	XP_005248404.1:p.His2933=
XM_005248349.2:c.8690A=	XP_005248406.1:p.His2897=
XM_005248350.2:c.8672A=	XP_005248407.1:p.His2891=
XM_005248353.3:c.5444A=	XP_005248410.1:p.His1815=
XM_006714489.2:c.8801A=	XP_006714552.1:p.His2934=
XM_006714491.2:c.3374A=	XP_006714554.1:p.His1125=
XM_011514085.1:c.8801A=	XP_011512387.1:p.His2934=
XM_011514086.1:c.8801A=	XP_011512388.1:p.His2934=
XM_011514087.1:c.8747A=	XP_011512389.1:p.His2916=
XM_011514088.1:c.8693A=	XP_011512390.1:p.His2898=
XM_011514089.1:c.8801A=	XP_011512391.1:p.His2934=
XM_011514090.1:c.8483A=	XP_011512392.1:p.His2828=
XM_011514091.1:c.8129A=	XP_011512393.1:p.His2710=
XM_011514092.1:c.8801A=	XP_011512394.1:p.His2934=
XM_011514094.1:c.6026A=	XP_011512396.1:p.His2009=
XR_427661.2:n.8976A=
XR_925644.1:n.8976A=
XM_005248345.4:c.8801A=	XP_005248402.1:p.His2934=
XM_005248346.4:c.8798A=	XP_005248403.1:p.His2933=
XM_005248347.4:c.8798A=	XP_005248404.1:p.His2933=
XM_005248349.4:c.8690A=	XP_005248406.1:p.His2897=
XM_005248350.4:c.8672A=	XP_005248407.1:p.His2891=
XM_006714491.3:c.3374A=	XP_006714554.1:p.His1125=
XM_011514085.3:c.8801A=	XP_011512387.1:p.His2934=
XM_011514086.3:c.8801A=	XP_011512388.1:p.His2934=
XM_011514087.2:c.8747A=	XP_011512389.1:p.His2916=
XM_011514088.2:c.8693A=	XP_011512390.1:p.His2898=
XM_011514089.2:c.8801A=	XP_011512391.1:p.His2934=
XM_011514090.3:c.8483A=	XP_011512392.1:p.His2828=
XM_011514092.2:c.8801A=	XP_011512394.1:p.His2934=
XM_011514094.2:c.6026A=	XP_011512396.1:p.His2009=
XM_017009760.1:c.8612A=	XP_016865249.1:p.His2871=
XM_017009761.2:c.8612A=	XP_016865250.1:p.His2871=
XM_017009763.1:c.7808A=	XP_016865252.1:p.His2603=
XM_017009765.1:c.7613A=	XP_016865254.1:p.His2538=
XM_017009766.1:c.5444A=	XP_016865255.1:p.His1815=
XM_024446183.1:c.8612A=	XP_024301951.1:p.His2871=
XM_024446184.1:c.8483A=	XP_024301952.1:p.His2828=
XM_024446185.1:c.8129A=	XP_024301953.1:p.His2710=
XM_024446186.1:c.7808A=	XP_024301954.1:p.His2603=
XR_001742208.1:n.8970A=
XR_925644.2:n.9025A=
NM_001384732.1:c.8801A= MANE Select	NP_001371661.1:p.His2934=
NM_023073.4:c.8639A=	NP_075561.3:p.His2880=