Canonical Allele Identifier: CA359474410

Gene: CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37154084G>C (hg19) ; chr5:g.37153982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153982G>C , CM000667.2:g.37153982G>C	GRCh38
NC_000005.9:g.37154084G>C , CM000667.1:g.37154084G>C	GRCh37
NC_000005.8:g.37189841G>C	NCBI36
NG_032772.1:g.100447C>G
NG_032772.2:g.100447C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1130C>G
ENST00000651892.2:c.8131C>G MANE Select	ENSP00000498265.2:p.Pro2711Ala
ENST00000425232.6:c.7969C>G	ENSP00000389014.2:p.Pro2657Ala
ENST00000508244.5:c.7969C>G	ENSP00000421690.1:p.Pro2657Ala
ENST00000509849.5:c.5143C>G	ENSP00000426337.1:p.Pro1715Ala
ENST00000509957.5:n.373C>G
ENST00000511210.5:n.422C>G
ENST00000511824.2:c.1245C>G
ENST00000514429.5:c.5167C>G	ENSP00000424223.1:p.Pro1723Ala
ENST00000515380.1:n.383C>G
NM_023073.3:c.7969C>G	NP_075561.3:p.Pro2657Ala
XM_005248345.2:c.8131C>G	XP_005248402.1:p.Pro2711Ala
XM_005248346.2:c.8128C>G	XP_005248403.1:p.Pro2710Ala
XM_005248347.2:c.8128C>G	XP_005248404.1:p.Pro2710Ala
XM_005248349.2:c.8020C>G	XP_005248406.1:p.Pro2674Ala
XM_005248350.2:c.8002C>G	XP_005248407.1:p.Pro2668Ala
XM_005248353.3:c.4774C>G	XP_005248410.1:p.Pro1592Ala
XM_006714489.2:c.8131C>G	XP_006714552.1:p.Pro2711Ala
XM_006714491.2:c.2704C>G	XP_006714554.1:p.Pro902Ala
XM_011514085.1:c.8131C>G	XP_011512387.1:p.Pro2711Ala
XM_011514086.1:c.8131C>G	XP_011512388.1:p.Pro2711Ala
XM_011514087.1:c.8077C>G	XP_011512389.1:p.Pro2693Ala
XM_011514088.1:c.8023C>G	XP_011512390.1:p.Pro2675Ala
XM_011514089.1:c.8131C>G	XP_011512391.1:p.Pro2711Ala
XM_011514090.1:c.7813C>G	XP_011512392.1:p.Pro2605Ala
XM_011514091.1:c.7459C>G	XP_011512393.1:p.Pro2487Ala
XM_011514092.1:c.8131C>G	XP_011512394.1:p.Pro2711Ala
XM_011514094.1:c.5356C>G	XP_011512396.1:p.Pro1786Ala
XR_427661.2:n.8306C>G
XR_925644.1:n.8306C>G
XM_005248345.4:c.8131C>G	XP_005248402.1:p.Pro2711Ala
XM_005248346.4:c.8128C>G	XP_005248403.1:p.Pro2710Ala
XM_005248347.4:c.8128C>G	XP_005248404.1:p.Pro2710Ala
XM_005248349.4:c.8020C>G	XP_005248406.1:p.Pro2674Ala
XM_005248350.4:c.8002C>G	XP_005248407.1:p.Pro2668Ala
XM_006714491.3:c.2704C>G	XP_006714554.1:p.Pro902Ala
XM_011514085.3:c.8131C>G	XP_011512387.1:p.Pro2711Ala
XM_011514086.3:c.8131C>G	XP_011512388.1:p.Pro2711Ala
XM_011514087.2:c.8077C>G	XP_011512389.1:p.Pro2693Ala
XM_011514088.2:c.8023C>G	XP_011512390.1:p.Pro2675Ala
XM_011514089.2:c.8131C>G	XP_011512391.1:p.Pro2711Ala
XM_011514090.3:c.7813C>G	XP_011512392.1:p.Pro2605Ala
XM_011514092.2:c.8131C>G	XP_011512394.1:p.Pro2711Ala
XM_011514094.2:c.5356C>G	XP_011512396.1:p.Pro1786Ala
XM_017009760.1:c.7942C>G	XP_016865249.1:p.Pro2648Ala
XM_017009761.2:c.7942C>G	XP_016865250.1:p.Pro2648Ala
XM_017009763.1:c.7138C>G	XP_016865252.1:p.Pro2380Ala
XM_017009765.1:c.6943C>G	XP_016865254.1:p.Pro2315Ala
XM_017009766.1:c.4774C>G	XP_016865255.1:p.Pro1592Ala
XM_024446183.1:c.7942C>G	XP_024301951.1:p.Pro2648Ala
XM_024446184.1:c.7813C>G	XP_024301952.1:p.Pro2605Ala
XM_024446185.1:c.7459C>G	XP_024301953.1:p.Pro2487Ala
XM_024446186.1:c.7138C>G	XP_024301954.1:p.Pro2380Ala
XR_001742208.1:n.8300C>G
XR_002956171.1:n.8246C>G
XR_925644.2:n.8355C>G
NM_001384732.1:c.8131C>G MANE Select	NP_001371661.1:p.Pro2711Ala
NM_023073.4:c.7969C>G	NP_075561.3:p.Pro2657Ala