Canonical Allele Identifier: CA359474377

Gene: CPLANE1

Linked Data

• gnomAD v4: 5-37153973-G-C
• MyVariant Identifiers: chr5:g.37154075G>C (hg19) ; chr5:g.37153973G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153973G>C , CM000667.2:g.37153973G>C	GRCh38
NC_000005.9:g.37154075G>C , CM000667.1:g.37154075G>C	GRCh37
NC_000005.8:g.37189832G>C	NCBI36
NG_032772.1:g.100456C>G
NG_032772.2:g.100456C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1139C>G
ENST00000651892.2:c.8140C>G MANE Select	ENSP00000498265.2:p.Arg2714Gly
ENST00000425232.6:c.7978C>G	ENSP00000389014.2:p.Arg2660Gly
ENST00000508244.5:c.7978C>G	ENSP00000421690.1:p.Arg2660Gly
ENST00000509849.5:c.5152C>G	ENSP00000426337.1:p.Arg1718Gly
ENST00000509957.5:n.382C>G
ENST00000511210.5:n.431C>G
ENST00000511824.2:c.1254C>G
ENST00000514429.5:c.5176C>G	ENSP00000424223.1:p.Arg1726Gly
ENST00000515380.1:n.392C>G
NM_023073.3:c.7978C>G	NP_075561.3:p.Arg2660Gly
XM_005248345.2:c.8140C>G	XP_005248402.1:p.Arg2714Gly
XM_005248346.2:c.8137C>G	XP_005248403.1:p.Arg2713Gly
XM_005248347.2:c.8137C>G	XP_005248404.1:p.Arg2713Gly
XM_005248349.2:c.8029C>G	XP_005248406.1:p.Arg2677Gly
XM_005248350.2:c.8011C>G	XP_005248407.1:p.Arg2671Gly
XM_005248353.3:c.4783C>G	XP_005248410.1:p.Arg1595Gly
XM_006714489.2:c.8140C>G	XP_006714552.1:p.Arg2714Gly
XM_006714491.2:c.2713C>G	XP_006714554.1:p.Arg905Gly
XM_011514085.1:c.8140C>G	XP_011512387.1:p.Arg2714Gly
XM_011514086.1:c.8140C>G	XP_011512388.1:p.Arg2714Gly
XM_011514087.1:c.8086C>G	XP_011512389.1:p.Arg2696Gly
XM_011514088.1:c.8032C>G	XP_011512390.1:p.Arg2678Gly
XM_011514089.1:c.8140C>G	XP_011512391.1:p.Arg2714Gly
XM_011514090.1:c.7822C>G	XP_011512392.1:p.Arg2608Gly
XM_011514091.1:c.7468C>G	XP_011512393.1:p.Arg2490Gly
XM_011514092.1:c.8140C>G	XP_011512394.1:p.Arg2714Gly
XM_011514094.1:c.5365C>G	XP_011512396.1:p.Arg1789Gly
XR_427661.2:n.8315C>G
XR_925644.1:n.8315C>G
XM_005248345.4:c.8140C>G	XP_005248402.1:p.Arg2714Gly
XM_005248346.4:c.8137C>G	XP_005248403.1:p.Arg2713Gly
XM_005248347.4:c.8137C>G	XP_005248404.1:p.Arg2713Gly
XM_005248349.4:c.8029C>G	XP_005248406.1:p.Arg2677Gly
XM_005248350.4:c.8011C>G	XP_005248407.1:p.Arg2671Gly
XM_006714491.3:c.2713C>G	XP_006714554.1:p.Arg905Gly
XM_011514085.3:c.8140C>G	XP_011512387.1:p.Arg2714Gly
XM_011514086.3:c.8140C>G	XP_011512388.1:p.Arg2714Gly
XM_011514087.2:c.8086C>G	XP_011512389.1:p.Arg2696Gly
XM_011514088.2:c.8032C>G	XP_011512390.1:p.Arg2678Gly
XM_011514089.2:c.8140C>G	XP_011512391.1:p.Arg2714Gly
XM_011514090.3:c.7822C>G	XP_011512392.1:p.Arg2608Gly
XM_011514092.2:c.8140C>G	XP_011512394.1:p.Arg2714Gly
XM_011514094.2:c.5365C>G	XP_011512396.1:p.Arg1789Gly
XM_017009760.1:c.7951C>G	XP_016865249.1:p.Arg2651Gly
XM_017009761.2:c.7951C>G	XP_016865250.1:p.Arg2651Gly
XM_017009763.1:c.7147C>G	XP_016865252.1:p.Arg2383Gly
XM_017009765.1:c.6952C>G	XP_016865254.1:p.Arg2318Gly
XM_017009766.1:c.4783C>G	XP_016865255.1:p.Arg1595Gly
XM_024446183.1:c.7951C>G	XP_024301951.1:p.Arg2651Gly
XM_024446184.1:c.7822C>G	XP_024301952.1:p.Arg2608Gly
XM_024446185.1:c.7468C>G	XP_024301953.1:p.Arg2490Gly
XM_024446186.1:c.7147C>G	XP_024301954.1:p.Arg2383Gly
XR_001742208.1:n.8309C>G
XR_002956171.1:n.8255C>G
XR_925644.2:n.8364C>G
NM_001384732.1:c.8140C>G MANE Select	NP_001371661.1:p.Arg2714Gly
NM_023073.4:c.7978C>G	NP_075561.3:p.Arg2660Gly