Canonical Allele Identifier: CA359474265

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154045A>T (hg19) ; chr5:g.37153943A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153943A>T , CM000667.2:g.37153943A>T	GRCh38
NC_000005.9:g.37154045A>T , CM000667.1:g.37154045A>T	GRCh37
NC_000005.8:g.37189802A>T	NCBI36
NG_032772.1:g.100486T>A
NG_032772.2:g.100486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1169T>A
ENST00000651892.2:c.8170T>A MANE Select	ENSP00000498265.2:p.Ser2724Thr
ENST00000425232.6:c.8008T>A	ENSP00000389014.2:p.Ser2670Thr
ENST00000508244.5:c.8008T>A	ENSP00000421690.1:p.Ser2670Thr
ENST00000509849.5:c.5182T>A	ENSP00000426337.1:p.Ser1728Thr
ENST00000509957.5:n.412T>A
ENST00000511210.5:n.461T>A
ENST00000511824.2:c.1284T>A
ENST00000514429.5:c.5206T>A	ENSP00000424223.1:p.Ser1736Thr
ENST00000515380.1:n.422T>A
NM_023073.3:c.8008T>A	NP_075561.3:p.Ser2670Thr
XM_005248345.2:c.8170T>A	XP_005248402.1:p.Ser2724Thr
XM_005248346.2:c.8167T>A	XP_005248403.1:p.Ser2723Thr
XM_005248347.2:c.8167T>A	XP_005248404.1:p.Ser2723Thr
XM_005248349.2:c.8059T>A	XP_005248406.1:p.Ser2687Thr
XM_005248350.2:c.8041T>A	XP_005248407.1:p.Ser2681Thr
XM_005248353.3:c.4813T>A	XP_005248410.1:p.Ser1605Thr
XM_006714489.2:c.8170T>A	XP_006714552.1:p.Ser2724Thr
XM_006714491.2:c.2743T>A	XP_006714554.1:p.Ser915Thr
XM_011514085.1:c.8170T>A	XP_011512387.1:p.Ser2724Thr
XM_011514086.1:c.8170T>A	XP_011512388.1:p.Ser2724Thr
XM_011514087.1:c.8116T>A	XP_011512389.1:p.Ser2706Thr
XM_011514088.1:c.8062T>A	XP_011512390.1:p.Ser2688Thr
XM_011514089.1:c.8170T>A	XP_011512391.1:p.Ser2724Thr
XM_011514090.1:c.7852T>A	XP_011512392.1:p.Ser2618Thr
XM_011514091.1:c.7498T>A	XP_011512393.1:p.Ser2500Thr
XM_011514092.1:c.8170T>A	XP_011512394.1:p.Ser2724Thr
XM_011514094.1:c.5395T>A	XP_011512396.1:p.Ser1799Thr
XR_427661.2:n.8345T>A
XR_925644.1:n.8345T>A
XM_005248345.4:c.8170T>A	XP_005248402.1:p.Ser2724Thr
XM_005248346.4:c.8167T>A	XP_005248403.1:p.Ser2723Thr
XM_005248347.4:c.8167T>A	XP_005248404.1:p.Ser2723Thr
XM_005248349.4:c.8059T>A	XP_005248406.1:p.Ser2687Thr
XM_005248350.4:c.8041T>A	XP_005248407.1:p.Ser2681Thr
XM_006714491.3:c.2743T>A	XP_006714554.1:p.Ser915Thr
XM_011514085.3:c.8170T>A	XP_011512387.1:p.Ser2724Thr
XM_011514086.3:c.8170T>A	XP_011512388.1:p.Ser2724Thr
XM_011514087.2:c.8116T>A	XP_011512389.1:p.Ser2706Thr
XM_011514088.2:c.8062T>A	XP_011512390.1:p.Ser2688Thr
XM_011514089.2:c.8170T>A	XP_011512391.1:p.Ser2724Thr
XM_011514090.3:c.7852T>A	XP_011512392.1:p.Ser2618Thr
XM_011514092.2:c.8170T>A	XP_011512394.1:p.Ser2724Thr
XM_011514094.2:c.5395T>A	XP_011512396.1:p.Ser1799Thr
XM_017009760.1:c.7981T>A	XP_016865249.1:p.Ser2661Thr
XM_017009761.2:c.7981T>A	XP_016865250.1:p.Ser2661Thr
XM_017009763.1:c.7177T>A	XP_016865252.1:p.Ser2393Thr
XM_017009765.1:c.6982T>A	XP_016865254.1:p.Ser2328Thr
XM_017009766.1:c.4813T>A	XP_016865255.1:p.Ser1605Thr
XM_024446183.1:c.7981T>A	XP_024301951.1:p.Ser2661Thr
XM_024446184.1:c.7852T>A	XP_024301952.1:p.Ser2618Thr
XM_024446185.1:c.7498T>A	XP_024301953.1:p.Ser2500Thr
XM_024446186.1:c.7177T>A	XP_024301954.1:p.Ser2393Thr
XR_001742208.1:n.8339T>A
XR_002956171.1:n.8285T>A
XR_925644.2:n.8394T>A
NM_001384732.1:c.8170T>A MANE Select	NP_001371661.1:p.Ser2724Thr
NM_023073.4:c.8008T>A	NP_075561.3:p.Ser2670Thr