Canonical Allele Identifier: CA359474332

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154063G>C (hg19) ; chr5:g.37153961G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153961G>C , CM000667.2:g.37153961G>C	GRCh38
NC_000005.9:g.37154063G>C , CM000667.1:g.37154063G>C	GRCh37
NC_000005.8:g.37189820G>C	NCBI36
NG_032772.1:g.100468C>G
NG_032772.2:g.100468C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1151C>G
ENST00000651892.2:c.8152C>G MANE Select	ENSP00000498265.2:p.Gln2718Glu
ENST00000425232.6:c.7990C>G	ENSP00000389014.2:p.Gln2664Glu
ENST00000508244.5:c.7990C>G	ENSP00000421690.1:p.Gln2664Glu
ENST00000509849.5:c.5164C>G	ENSP00000426337.1:p.Gln1722Glu
ENST00000509957.5:n.394C>G
ENST00000511210.5:n.443C>G
ENST00000511824.2:c.1266C>G
ENST00000514429.5:c.5188C>G	ENSP00000424223.1:p.Gln1730Glu
ENST00000515380.1:n.404C>G
NM_023073.3:c.7990C>G	NP_075561.3:p.Gln2664Glu
XM_005248345.2:c.8152C>G	XP_005248402.1:p.Gln2718Glu
XM_005248346.2:c.8149C>G	XP_005248403.1:p.Gln2717Glu
XM_005248347.2:c.8149C>G	XP_005248404.1:p.Gln2717Glu
XM_005248349.2:c.8041C>G	XP_005248406.1:p.Gln2681Glu
XM_005248350.2:c.8023C>G	XP_005248407.1:p.Gln2675Glu
XM_005248353.3:c.4795C>G	XP_005248410.1:p.Gln1599Glu
XM_006714489.2:c.8152C>G	XP_006714552.1:p.Gln2718Glu
XM_006714491.2:c.2725C>G	XP_006714554.1:p.Gln909Glu
XM_011514085.1:c.8152C>G	XP_011512387.1:p.Gln2718Glu
XM_011514086.1:c.8152C>G	XP_011512388.1:p.Gln2718Glu
XM_011514087.1:c.8098C>G	XP_011512389.1:p.Gln2700Glu
XM_011514088.1:c.8044C>G	XP_011512390.1:p.Gln2682Glu
XM_011514089.1:c.8152C>G	XP_011512391.1:p.Gln2718Glu
XM_011514090.1:c.7834C>G	XP_011512392.1:p.Gln2612Glu
XM_011514091.1:c.7480C>G	XP_011512393.1:p.Gln2494Glu
XM_011514092.1:c.8152C>G	XP_011512394.1:p.Gln2718Glu
XM_011514094.1:c.5377C>G	XP_011512396.1:p.Gln1793Glu
XR_427661.2:n.8327C>G
XR_925644.1:n.8327C>G
XM_005248345.4:c.8152C>G	XP_005248402.1:p.Gln2718Glu
XM_005248346.4:c.8149C>G	XP_005248403.1:p.Gln2717Glu
XM_005248347.4:c.8149C>G	XP_005248404.1:p.Gln2717Glu
XM_005248349.4:c.8041C>G	XP_005248406.1:p.Gln2681Glu
XM_005248350.4:c.8023C>G	XP_005248407.1:p.Gln2675Glu
XM_006714491.3:c.2725C>G	XP_006714554.1:p.Gln909Glu
XM_011514085.3:c.8152C>G	XP_011512387.1:p.Gln2718Glu
XM_011514086.3:c.8152C>G	XP_011512388.1:p.Gln2718Glu
XM_011514087.2:c.8098C>G	XP_011512389.1:p.Gln2700Glu
XM_011514088.2:c.8044C>G	XP_011512390.1:p.Gln2682Glu
XM_011514089.2:c.8152C>G	XP_011512391.1:p.Gln2718Glu
XM_011514090.3:c.7834C>G	XP_011512392.1:p.Gln2612Glu
XM_011514092.2:c.8152C>G	XP_011512394.1:p.Gln2718Glu
XM_011514094.2:c.5377C>G	XP_011512396.1:p.Gln1793Glu
XM_017009760.1:c.7963C>G	XP_016865249.1:p.Gln2655Glu
XM_017009761.2:c.7963C>G	XP_016865250.1:p.Gln2655Glu
XM_017009763.1:c.7159C>G	XP_016865252.1:p.Gln2387Glu
XM_017009765.1:c.6964C>G	XP_016865254.1:p.Gln2322Glu
XM_017009766.1:c.4795C>G	XP_016865255.1:p.Gln1599Glu
XM_024446183.1:c.7963C>G	XP_024301951.1:p.Gln2655Glu
XM_024446184.1:c.7834C>G	XP_024301952.1:p.Gln2612Glu
XM_024446185.1:c.7480C>G	XP_024301953.1:p.Gln2494Glu
XM_024446186.1:c.7159C>G	XP_024301954.1:p.Gln2387Glu
XR_001742208.1:n.8321C>G
XR_002956171.1:n.8267C>G
XR_925644.2:n.8376C>G
NM_001384732.1:c.8152C>G MANE Select	NP_001371661.1:p.Gln2718Glu
NM_023073.4:c.7990C>G	NP_075561.3:p.Gln2664Glu