Canonical Allele Identifier: CA2673584427

Gene: CPLANE1

Linked Data

• gnomAD v4: 5-37157372-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37157372G>C , CM000667.2:g.37157372G>C	GRCh38
NC_000005.9:g.37157474G>C , CM000667.1:g.37157474G>C	GRCh37
NC_000005.8:g.37193231G>C	NCBI36
NG_032772.1:g.97057C>G
NG_032772.2:g.97057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1059C>G
ENST00000651892.2:c.8060C>G MANE Select	ENSP00000498265.2:p.Thr2687Arg
ENST00000425232.6:c.7957+298C>G	ENSP00000389014.2:n.7957+298C>G
ENST00000508244.5:c.7957+298C>G	ENSP00000421690.1:n.7957+298C>G
ENST00000509849.5:c.5072C>G	ENSP00000426337.1:p.Thr1691Arg
ENST00000509957.5:n.302C>G
ENST00000511210.5:n.351C>G
ENST00000511824.2:c.1174C>G
ENST00000514429.5:c.5155+298C>G	ENSP00000424223.1:n.5155+298C>G
ENST00000515380.1:n.312C>G
NM_023073.3:c.7957+298C>G	NP_075561.3:n.7957+298C>G
XM_005248345.2:c.8060C>G	XP_005248402.1:p.Thr2687Arg
XM_005248346.2:c.8057C>G	XP_005248403.1:p.Thr2686Arg
XM_005248347.2:c.8057C>G	XP_005248404.1:p.Thr2686Arg
XM_005248349.2:c.8008+298C>G	XP_005248406.1:n.8008+298C>G
XM_005248350.2:c.7931C>G	XP_005248407.1:p.Thr2644Arg
XM_005248353.3:c.4703C>G	XP_005248410.1:p.Thr1568Arg
XM_006714489.2:c.8060C>G	XP_006714552.1:p.Thr2687Arg
XM_006714491.2:c.2633C>G	XP_006714554.1:p.Thr878Arg
XM_011514085.1:c.8060C>G	XP_011512387.1:p.Thr2687Arg
XM_011514086.1:c.8060C>G	XP_011512388.1:p.Thr2687Arg
XM_011514087.1:c.8006C>G	XP_011512389.1:p.Thr2669Arg
XM_011514088.1:c.8011+298C>G	XP_011512390.1:n.8011+298C>G
XM_011514089.1:c.8060C>G	XP_011512391.1:p.Thr2687Arg
XM_011514090.1:c.7742C>G	XP_011512392.1:p.Thr2581Arg
XM_011514091.1:c.7388C>G	XP_011512393.1:p.Thr2463Arg
XM_011514092.1:c.8060C>G	XP_011512394.1:p.Thr2687Arg
XM_011514094.1:c.5285C>G	XP_011512396.1:p.Thr1762Arg
XR_427661.2:n.8235C>G
XR_925644.1:n.8235C>G
XM_005248345.4:c.8060C>G	XP_005248402.1:p.Thr2687Arg
XM_005248346.4:c.8057C>G	XP_005248403.1:p.Thr2686Arg
XM_005248347.4:c.8057C>G	XP_005248404.1:p.Thr2686Arg
XM_005248349.4:c.8008+298C>G	XP_005248406.1:n.8008+298C>G
XM_005248350.4:c.7931C>G	XP_005248407.1:p.Thr2644Arg
XM_006714491.3:c.2633C>G	XP_006714554.1:p.Thr878Arg
XM_011514085.3:c.8060C>G	XP_011512387.1:p.Thr2687Arg
XM_011514086.3:c.8060C>G	XP_011512388.1:p.Thr2687Arg
XM_011514087.2:c.8006C>G	XP_011512389.1:p.Thr2669Arg
XM_011514088.2:c.8011+298C>G	XP_011512390.1:n.8011+298C>G
XM_011514089.2:c.8060C>G	XP_011512391.1:p.Thr2687Arg
XM_011514090.3:c.7742C>G	XP_011512392.1:p.Thr2581Arg
XM_011514092.2:c.8060C>G	XP_011512394.1:p.Thr2687Arg
XM_011514094.2:c.5285C>G	XP_011512396.1:p.Thr1762Arg
XM_017009760.1:c.7871C>G	XP_016865249.1:p.Thr2624Arg
XM_017009761.2:c.7871C>G	XP_016865250.1:p.Thr2624Arg
XM_017009763.1:c.7067C>G	XP_016865252.1:p.Thr2356Arg
XM_017009765.1:c.6872C>G	XP_016865254.1:p.Thr2291Arg
XM_017009766.1:c.4703C>G	XP_016865255.1:p.Thr1568Arg
XM_024446183.1:c.7871C>G	XP_024301951.1:p.Thr2624Arg
XM_024446184.1:c.7742C>G	XP_024301952.1:p.Thr2581Arg
XM_024446185.1:c.7388C>G	XP_024301953.1:p.Thr2463Arg
XM_024446186.1:c.7067C>G	XP_024301954.1:p.Thr2356Arg
XR_001742208.1:n.8229C>G
XR_002956171.1:n.8175C>G
XR_925644.2:n.8284C>G
NM_001384732.1:c.8060C>G MANE Select	NP_001371661.1:p.Thr2687Arg
NM_023073.4:c.7957+298C>G	NP_075561.3:n.7957+298C>G