Canonical Allele Identifier: CA444096646

Gene: CPLANE1

Linked Data

• gnomAD v4: 5-37153812-T-C
• MyVariant Identifiers: chr5:g.37153914T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37153812T>C , CM000667.2:g.37153812T>C	GRCh38
NC_000005.9:g.37153914T>C , CM000667.1:g.37153914T>C	GRCh37
NC_000005.8:g.37189671T>C	NCBI36
NG_032772.1:g.100617A>G
NG_032772.2:g.100617A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1300A>G
ENST00000651892.2:c.8301A>G MANE Select	ENSP00000498265.2:p.Ala2767=
ENST00000425232.6:c.8139A>G	ENSP00000389014.2:p.Ala2713=
ENST00000508244.5:c.8139A>G	ENSP00000421690.1:p.Ala2713=
ENST00000508405.1:n.33A>G
ENST00000509849.5:c.5313A>G	ENSP00000426337.1:p.Ala1771=
ENST00000509957.5:n.543A>G
ENST00000511824.2:c.1415A>G
ENST00000514429.5:c.5337A>G	ENSP00000424223.1:p.Ala1779=
NM_023073.3:c.8139A>G	NP_075561.3:p.Ala2713=
XM_005248345.2:c.8301A>G	XP_005248402.1:p.Ala2767=
XM_005248346.2:c.8298A>G	XP_005248403.1:p.Ala2766=
XM_005248347.2:c.8298A>G	XP_005248404.1:p.Ala2766=
XM_005248349.2:c.8190A>G	XP_005248406.1:p.Ala2730=
XM_005248350.2:c.8172A>G	XP_005248407.1:p.Ala2724=
XM_005248353.3:c.4944A>G	XP_005248410.1:p.Ala1648=
XM_006714489.2:c.8301A>G	XP_006714552.1:p.Ala2767=
XM_006714491.2:c.2874A>G	XP_006714554.1:p.Ala958=
XM_011514085.1:c.8301A>G	XP_011512387.1:p.Ala2767=
XM_011514086.1:c.8301A>G	XP_011512388.1:p.Ala2767=
XM_011514087.1:c.8247A>G	XP_011512389.1:p.Ala2749=
XM_011514088.1:c.8193A>G	XP_011512390.1:p.Ala2731=
XM_011514089.1:c.8301A>G	XP_011512391.1:p.Ala2767=
XM_011514090.1:c.7983A>G	XP_011512392.1:p.Ala2661=
XM_011514091.1:c.7629A>G	XP_011512393.1:p.Ala2543=
XM_011514092.1:c.8301A>G	XP_011512394.1:p.Ala2767=
XM_011514094.1:c.5526A>G	XP_011512396.1:p.Ala1842=
XR_427661.2:n.8476A>G
XR_925644.1:n.8476A>G
XM_005248345.4:c.8301A>G	XP_005248402.1:p.Ala2767=
XM_005248346.4:c.8298A>G	XP_005248403.1:p.Ala2766=
XM_005248347.4:c.8298A>G	XP_005248404.1:p.Ala2766=
XM_005248349.4:c.8190A>G	XP_005248406.1:p.Ala2730=
XM_005248350.4:c.8172A>G	XP_005248407.1:p.Ala2724=
XM_006714491.3:c.2874A>G	XP_006714554.1:p.Ala958=
XM_011514085.3:c.8301A>G	XP_011512387.1:p.Ala2767=
XM_011514086.3:c.8301A>G	XP_011512388.1:p.Ala2767=
XM_011514087.2:c.8247A>G	XP_011512389.1:p.Ala2749=
XM_011514088.2:c.8193A>G	XP_011512390.1:p.Ala2731=
XM_011514089.2:c.8301A>G	XP_011512391.1:p.Ala2767=
XM_011514090.3:c.7983A>G	XP_011512392.1:p.Ala2661=
XM_011514092.2:c.8301A>G	XP_011512394.1:p.Ala2767=
XM_011514094.2:c.5526A>G	XP_011512396.1:p.Ala1842=
XM_017009760.1:c.8112A>G	XP_016865249.1:p.Ala2704=
XM_017009761.2:c.8112A>G	XP_016865250.1:p.Ala2704=
XM_017009763.1:c.7308A>G	XP_016865252.1:p.Ala2436=
XM_017009765.1:c.7113A>G	XP_016865254.1:p.Ala2371=
XM_017009766.1:c.4944A>G	XP_016865255.1:p.Ala1648=
XM_024446183.1:c.8112A>G	XP_024301951.1:p.Ala2704=
XM_024446184.1:c.7983A>G	XP_024301952.1:p.Ala2661=
XM_024446185.1:c.7629A>G	XP_024301953.1:p.Ala2543=
XM_024446186.1:c.7308A>G	XP_024301954.1:p.Ala2436=
XR_001742208.1:n.8470A>G
XR_002956171.1:n.8416A>G
XR_925644.2:n.8525A>G
NM_001384732.1:c.8301A>G MANE Select	NP_001371661.1:p.Ala2767=
NM_023073.4:c.8139A>G	NP_075561.3:p.Ala2713=