Canonical Allele Identifier: CA359498421

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37125361A>T (hg19) ; chr5:g.37125259A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125259A>T , CM000667.2:g.37125259A>T	GRCh38
NC_000005.9:g.37125361A>T , CM000667.1:g.37125361A>T	GRCh37
NC_000005.8:g.37161118A>T	NCBI36
NG_032772.1:g.129170T>A
NG_032772.2:g.129170T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1942T>A
ENST00000651892.2:c.8943T>A MANE Select	ENSP00000498265.2:p.Cys2981Ter
ENST00000676160.1:n.804T>A
ENST00000425232.6:c.8781T>A	ENSP00000389014.2:p.Cys2927Ter
ENST00000508244.5:c.8781T>A	ENSP00000421690.1:p.Cys2927Ter
ENST00000509849.5:c.5955T>A	ENSP00000426337.1:n.5955T>A
ENST00000509957.5:n.4124T>A
ENST00000512288.5:n.342-3475T>A
ENST00000514429.5:c.5979T>A	ENSP00000424223.1:p.Cys1993Ter
NM_023073.3:c.8781T>A	NP_075561.3:p.Cys2927Ter
XM_005248345.2:c.8943T>A	XP_005248402.1:p.Cys2981Ter
XM_005248346.2:c.8940T>A	XP_005248403.1:p.Cys2980Ter
XM_005248347.2:c.8940T>A	XP_005248404.1:p.Cys2980Ter
XM_005248349.2:c.8832T>A	XP_005248406.1:p.Cys2944Ter
XM_005248350.2:c.8814T>A	XP_005248407.1:p.Cys2938Ter
XM_005248353.3:c.5586T>A	XP_005248410.1:p.Cys1862Ter
XM_006714489.2:c.8943T>A	XP_006714552.1:p.Cys2981Ter
XM_006714491.2:c.3516T>A	XP_006714554.1:p.Cys1172Ter
XM_011514085.1:c.8943T>A	XP_011512387.1:p.Cys2981Ter
XM_011514086.1:c.8943T>A	XP_011512388.1:p.Cys2981Ter
XM_011514087.1:c.8889T>A	XP_011512389.1:p.Cys2963Ter
XM_011514088.1:c.8835T>A	XP_011512390.1:p.Cys2945Ter
XM_011514089.1:c.8943T>A	XP_011512391.1:p.Cys2981Ter
XM_011514090.1:c.8625T>A	XP_011512392.1:p.Cys2875Ter
XM_011514091.1:c.8271T>A	XP_011512393.1:p.Cys2757Ter
XM_011514092.1:c.8943T>A	XP_011512394.1:p.Cys2981Ter
XM_011514094.1:c.6168T>A	XP_011512396.1:p.Cys2056Ter
XR_427661.2:n.9118T>A
XR_925644.1:n.9118T>A
XM_005248345.4:c.8943T>A	XP_005248402.1:p.Cys2981Ter
XM_005248346.4:c.8940T>A	XP_005248403.1:p.Cys2980Ter
XM_005248347.4:c.8940T>A	XP_005248404.1:p.Cys2980Ter
XM_005248349.4:c.8832T>A	XP_005248406.1:p.Cys2944Ter
XM_005248350.4:c.8814T>A	XP_005248407.1:p.Cys2938Ter
XM_006714491.3:c.3516T>A	XP_006714554.1:p.Cys1172Ter
XM_011514085.3:c.8943T>A	XP_011512387.1:p.Cys2981Ter
XM_011514086.3:c.8943T>A	XP_011512388.1:p.Cys2981Ter
XM_011514087.2:c.8889T>A	XP_011512389.1:p.Cys2963Ter
XM_011514088.2:c.8835T>A	XP_011512390.1:p.Cys2945Ter
XM_011514089.2:c.8943T>A	XP_011512391.1:p.Cys2981Ter
XM_011514090.3:c.8625T>A	XP_011512392.1:p.Cys2875Ter
XM_011514092.2:c.8943T>A	XP_011512394.1:p.Cys2981Ter
XM_011514094.2:c.6168T>A	XP_011512396.1:p.Cys2056Ter
XM_017009760.1:c.8754T>A	XP_016865249.1:p.Cys2918Ter
XM_017009761.2:c.8754T>A	XP_016865250.1:p.Cys2918Ter
XM_017009763.1:c.7950T>A	XP_016865252.1:p.Cys2650Ter
XM_017009765.1:c.7755T>A	XP_016865254.1:p.Cys2585Ter
XM_017009766.1:c.5586T>A	XP_016865255.1:p.Cys1862Ter
XM_024446183.1:c.8754T>A	XP_024301951.1:p.Cys2918Ter
XM_024446184.1:c.8625T>A	XP_024301952.1:p.Cys2875Ter
XM_024446185.1:c.8271T>A	XP_024301953.1:p.Cys2757Ter
XM_024446186.1:c.7950T>A	XP_024301954.1:p.Cys2650Ter
XR_925644.2:n.9167T>A
NM_001384732.1:c.8943T>A MANE Select	NP_001371661.1:p.Cys2981Ter
NM_023073.4:c.8781T>A	NP_075561.3:p.Cys2927Ter