Canonical Allele Identifier: CA359500038

Gene: CPLANE1

Linked Data

• gnomAD v4: 5-37125408-T-C
• MyVariant Identifiers: chr5:g.37125510T>C (hg19) ; chr5:g.37125408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37125408T>C , CM000667.2:g.37125408T>C	GRCh38
NC_000005.9:g.37125510T>C , CM000667.1:g.37125510T>C	GRCh37
NC_000005.8:g.37161267T>C	NCBI36
NG_032772.1:g.129021A>G
NG_032772.2:g.129021A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1793A>G
ENST00000651892.2:c.8794A>G MANE Select	ENSP00000498265.2:p.Ile2932Val
ENST00000676160.1:n.655A>G
ENST00000425232.6:c.8632A>G	ENSP00000389014.2:p.Ile2878Val
ENST00000508244.5:c.8632A>G	ENSP00000421690.1:p.Ile2878Val
ENST00000509849.5:c.5806A>G	ENSP00000426337.1:n.5806A>G
ENST00000509957.5:n.3975A>G
ENST00000512288.5:n.342-3624A>G
ENST00000514429.5:c.5830A>G	ENSP00000424223.1:p.Ile1944Val
NM_023073.3:c.8632A>G	NP_075561.3:p.Ile2878Val
XM_005248345.2:c.8794A>G	XP_005248402.1:p.Ile2932Val
XM_005248346.2:c.8791A>G	XP_005248403.1:p.Ile2931Val
XM_005248347.2:c.8791A>G	XP_005248404.1:p.Ile2931Val
XM_005248349.2:c.8683A>G	XP_005248406.1:p.Ile2895Val
XM_005248350.2:c.8665A>G	XP_005248407.1:p.Ile2889Val
XM_005248353.3:c.5437A>G	XP_005248410.1:p.Ile1813Val
XM_006714489.2:c.8794A>G	XP_006714552.1:p.Ile2932Val
XM_006714491.2:c.3367A>G	XP_006714554.1:p.Ile1123Val
XM_011514085.1:c.8794A>G	XP_011512387.1:p.Ile2932Val
XM_011514086.1:c.8794A>G	XP_011512388.1:p.Ile2932Val
XM_011514087.1:c.8740A>G	XP_011512389.1:p.Ile2914Val
XM_011514088.1:c.8686A>G	XP_011512390.1:p.Ile2896Val
XM_011514089.1:c.8794A>G	XP_011512391.1:p.Ile2932Val
XM_011514090.1:c.8476A>G	XP_011512392.1:p.Ile2826Val
XM_011514091.1:c.8122A>G	XP_011512393.1:p.Ile2708Val
XM_011514092.1:c.8794A>G	XP_011512394.1:p.Ile2932Val
XM_011514094.1:c.6019A>G	XP_011512396.1:p.Ile2007Val
XR_427661.2:n.8969A>G
XR_925644.1:n.8969A>G
XM_005248345.4:c.8794A>G	XP_005248402.1:p.Ile2932Val
XM_005248346.4:c.8791A>G	XP_005248403.1:p.Ile2931Val
XM_005248347.4:c.8791A>G	XP_005248404.1:p.Ile2931Val
XM_005248349.4:c.8683A>G	XP_005248406.1:p.Ile2895Val
XM_005248350.4:c.8665A>G	XP_005248407.1:p.Ile2889Val
XM_006714491.3:c.3367A>G	XP_006714554.1:p.Ile1123Val
XM_011514085.3:c.8794A>G	XP_011512387.1:p.Ile2932Val
XM_011514086.3:c.8794A>G	XP_011512388.1:p.Ile2932Val
XM_011514087.2:c.8740A>G	XP_011512389.1:p.Ile2914Val
XM_011514088.2:c.8686A>G	XP_011512390.1:p.Ile2896Val
XM_011514089.2:c.8794A>G	XP_011512391.1:p.Ile2932Val
XM_011514090.3:c.8476A>G	XP_011512392.1:p.Ile2826Val
XM_011514092.2:c.8794A>G	XP_011512394.1:p.Ile2932Val
XM_011514094.2:c.6019A>G	XP_011512396.1:p.Ile2007Val
XM_017009760.1:c.8605A>G	XP_016865249.1:p.Ile2869Val
XM_017009761.2:c.8605A>G	XP_016865250.1:p.Ile2869Val
XM_017009763.1:c.7801A>G	XP_016865252.1:p.Ile2601Val
XM_017009765.1:c.7606A>G	XP_016865254.1:p.Ile2536Val
XM_017009766.1:c.5437A>G	XP_016865255.1:p.Ile1813Val
XM_024446183.1:c.8605A>G	XP_024301951.1:p.Ile2869Val
XM_024446184.1:c.8476A>G	XP_024301952.1:p.Ile2826Val
XM_024446185.1:c.8122A>G	XP_024301953.1:p.Ile2708Val
XM_024446186.1:c.7801A>G	XP_024301954.1:p.Ile2601Val
XR_001742208.1:n.8963A>G
XR_925644.2:n.9018A>G
NM_001384732.1:c.8794A>G MANE Select	NP_001371661.1:p.Ile2932Val
NM_023073.4:c.8632A>G	NP_075561.3:p.Ile2878Val