Canonical Allele Identifier: CA359473829

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37153925G>C (hg19) ; chr5:g.37153823G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153823G>C , CM000667.2:g.37153823G>C	GRCh38
NC_000005.9:g.37153925G>C , CM000667.1:g.37153925G>C	GRCh37
NC_000005.8:g.37189682G>C	NCBI36
NG_032772.1:g.100606C>G
NG_032772.2:g.100606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1289C>G
ENST00000651892.2:c.8290C>G MANE Select	ENSP00000498265.2:p.Gln2764Glu
ENST00000425232.6:c.8128C>G	ENSP00000389014.2:p.Gln2710Glu
ENST00000508244.5:c.8128C>G	ENSP00000421690.1:p.Gln2710Glu
ENST00000508405.1:n.22C>G
ENST00000509849.5:c.5302C>G	ENSP00000426337.1:p.Gln1768Glu
ENST00000509957.5:n.532C>G
ENST00000511824.2:c.1404C>G
ENST00000514429.5:c.5326C>G	ENSP00000424223.1:p.Gln1776Glu
NM_023073.3:c.8128C>G	NP_075561.3:p.Gln2710Glu
XM_005248345.2:c.8290C>G	XP_005248402.1:p.Gln2764Glu
XM_005248346.2:c.8287C>G	XP_005248403.1:p.Gln2763Glu
XM_005248347.2:c.8287C>G	XP_005248404.1:p.Gln2763Glu
XM_005248349.2:c.8179C>G	XP_005248406.1:p.Gln2727Glu
XM_005248350.2:c.8161C>G	XP_005248407.1:p.Gln2721Glu
XM_005248353.3:c.4933C>G	XP_005248410.1:p.Gln1645Glu
XM_006714489.2:c.8290C>G	XP_006714552.1:p.Gln2764Glu
XM_006714491.2:c.2863C>G	XP_006714554.1:p.Gln955Glu
XM_011514085.1:c.8290C>G	XP_011512387.1:p.Gln2764Glu
XM_011514086.1:c.8290C>G	XP_011512388.1:p.Gln2764Glu
XM_011514087.1:c.8236C>G	XP_011512389.1:p.Gln2746Glu
XM_011514088.1:c.8182C>G	XP_011512390.1:p.Gln2728Glu
XM_011514089.1:c.8290C>G	XP_011512391.1:p.Gln2764Glu
XM_011514090.1:c.7972C>G	XP_011512392.1:p.Gln2658Glu
XM_011514091.1:c.7618C>G	XP_011512393.1:p.Gln2540Glu
XM_011514092.1:c.8290C>G	XP_011512394.1:p.Gln2764Glu
XM_011514094.1:c.5515C>G	XP_011512396.1:p.Gln1839Glu
XR_427661.2:n.8465C>G
XR_925644.1:n.8465C>G
XM_005248345.4:c.8290C>G	XP_005248402.1:p.Gln2764Glu
XM_005248346.4:c.8287C>G	XP_005248403.1:p.Gln2763Glu
XM_005248347.4:c.8287C>G	XP_005248404.1:p.Gln2763Glu
XM_005248349.4:c.8179C>G	XP_005248406.1:p.Gln2727Glu
XM_005248350.4:c.8161C>G	XP_005248407.1:p.Gln2721Glu
XM_006714491.3:c.2863C>G	XP_006714554.1:p.Gln955Glu
XM_011514085.3:c.8290C>G	XP_011512387.1:p.Gln2764Glu
XM_011514086.3:c.8290C>G	XP_011512388.1:p.Gln2764Glu
XM_011514087.2:c.8236C>G	XP_011512389.1:p.Gln2746Glu
XM_011514088.2:c.8182C>G	XP_011512390.1:p.Gln2728Glu
XM_011514089.2:c.8290C>G	XP_011512391.1:p.Gln2764Glu
XM_011514090.3:c.7972C>G	XP_011512392.1:p.Gln2658Glu
XM_011514092.2:c.8290C>G	XP_011512394.1:p.Gln2764Glu
XM_011514094.2:c.5515C>G	XP_011512396.1:p.Gln1839Glu
XM_017009760.1:c.8101C>G	XP_016865249.1:p.Gln2701Glu
XM_017009761.2:c.8101C>G	XP_016865250.1:p.Gln2701Glu
XM_017009763.1:c.7297C>G	XP_016865252.1:p.Gln2433Glu
XM_017009765.1:c.7102C>G	XP_016865254.1:p.Gln2368Glu
XM_017009766.1:c.4933C>G	XP_016865255.1:p.Gln1645Glu
XM_024446183.1:c.8101C>G	XP_024301951.1:p.Gln2701Glu
XM_024446184.1:c.7972C>G	XP_024301952.1:p.Gln2658Glu
XM_024446185.1:c.7618C>G	XP_024301953.1:p.Gln2540Glu
XM_024446186.1:c.7297C>G	XP_024301954.1:p.Gln2433Glu
XR_001742208.1:n.8459C>G
XR_002956171.1:n.8405C>G
XR_925644.2:n.8514C>G
NM_001384732.1:c.8290C>G MANE Select	NP_001371661.1:p.Gln2764Glu
NM_023073.4:c.8128C>G	NP_075561.3:p.Gln2710Glu