Canonical Allele Identifier: CA359474364

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154071A>G (hg19) ; chr5:g.37153969A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153969A>G , CM000667.2:g.37153969A>G	GRCh38
NC_000005.9:g.37154071A>G , CM000667.1:g.37154071A>G	GRCh37
NC_000005.8:g.37189828A>G	NCBI36
NG_032772.1:g.100460T>C
NG_032772.2:g.100460T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1143T>C
ENST00000651892.2:c.8144T>C MANE Select	ENSP00000498265.2:p.Phe2715Ser
ENST00000425232.6:c.7982T>C	ENSP00000389014.2:p.Phe2661Ser
ENST00000508244.5:c.7982T>C	ENSP00000421690.1:p.Phe2661Ser
ENST00000509849.5:c.5156T>C	ENSP00000426337.1:p.Phe1719Ser
ENST00000509957.5:n.386T>C
ENST00000511210.5:n.435T>C
ENST00000511824.2:c.1258T>C
ENST00000514429.5:c.5180T>C	ENSP00000424223.1:p.Phe1727Ser
ENST00000515380.1:n.396T>C
NM_023073.3:c.7982T>C	NP_075561.3:p.Phe2661Ser
XM_005248345.2:c.8144T>C	XP_005248402.1:p.Phe2715Ser
XM_005248346.2:c.8141T>C	XP_005248403.1:p.Phe2714Ser
XM_005248347.2:c.8141T>C	XP_005248404.1:p.Phe2714Ser
XM_005248349.2:c.8033T>C	XP_005248406.1:p.Phe2678Ser
XM_005248350.2:c.8015T>C	XP_005248407.1:p.Phe2672Ser
XM_005248353.3:c.4787T>C	XP_005248410.1:p.Phe1596Ser
XM_006714489.2:c.8144T>C	XP_006714552.1:p.Phe2715Ser
XM_006714491.2:c.2717T>C	XP_006714554.1:p.Phe906Ser
XM_011514085.1:c.8144T>C	XP_011512387.1:p.Phe2715Ser
XM_011514086.1:c.8144T>C	XP_011512388.1:p.Phe2715Ser
XM_011514087.1:c.8090T>C	XP_011512389.1:p.Phe2697Ser
XM_011514088.1:c.8036T>C	XP_011512390.1:p.Phe2679Ser
XM_011514089.1:c.8144T>C	XP_011512391.1:p.Phe2715Ser
XM_011514090.1:c.7826T>C	XP_011512392.1:p.Phe2609Ser
XM_011514091.1:c.7472T>C	XP_011512393.1:p.Phe2491Ser
XM_011514092.1:c.8144T>C	XP_011512394.1:p.Phe2715Ser
XM_011514094.1:c.5369T>C	XP_011512396.1:p.Phe1790Ser
XR_427661.2:n.8319T>C
XR_925644.1:n.8319T>C
XM_005248345.4:c.8144T>C	XP_005248402.1:p.Phe2715Ser
XM_005248346.4:c.8141T>C	XP_005248403.1:p.Phe2714Ser
XM_005248347.4:c.8141T>C	XP_005248404.1:p.Phe2714Ser
XM_005248349.4:c.8033T>C	XP_005248406.1:p.Phe2678Ser
XM_005248350.4:c.8015T>C	XP_005248407.1:p.Phe2672Ser
XM_006714491.3:c.2717T>C	XP_006714554.1:p.Phe906Ser
XM_011514085.3:c.8144T>C	XP_011512387.1:p.Phe2715Ser
XM_011514086.3:c.8144T>C	XP_011512388.1:p.Phe2715Ser
XM_011514087.2:c.8090T>C	XP_011512389.1:p.Phe2697Ser
XM_011514088.2:c.8036T>C	XP_011512390.1:p.Phe2679Ser
XM_011514089.2:c.8144T>C	XP_011512391.1:p.Phe2715Ser
XM_011514090.3:c.7826T>C	XP_011512392.1:p.Phe2609Ser
XM_011514092.2:c.8144T>C	XP_011512394.1:p.Phe2715Ser
XM_011514094.2:c.5369T>C	XP_011512396.1:p.Phe1790Ser
XM_017009760.1:c.7955T>C	XP_016865249.1:p.Phe2652Ser
XM_017009761.2:c.7955T>C	XP_016865250.1:p.Phe2652Ser
XM_017009763.1:c.7151T>C	XP_016865252.1:p.Phe2384Ser
XM_017009765.1:c.6956T>C	XP_016865254.1:p.Phe2319Ser
XM_017009766.1:c.4787T>C	XP_016865255.1:p.Phe1596Ser
XM_024446183.1:c.7955T>C	XP_024301951.1:p.Phe2652Ser
XM_024446184.1:c.7826T>C	XP_024301952.1:p.Phe2609Ser
XM_024446185.1:c.7472T>C	XP_024301953.1:p.Phe2491Ser
XM_024446186.1:c.7151T>C	XP_024301954.1:p.Phe2384Ser
XR_001742208.1:n.8313T>C
XR_002956171.1:n.8259T>C
XR_925644.2:n.8368T>C
NM_001384732.1:c.8144T>C MANE Select	NP_001371661.1:p.Phe2715Ser
NM_023073.4:c.7982T>C	NP_075561.3:p.Phe2661Ser