Canonical Allele Identifier: CA2765914152

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154092_37154093insAGAG , CM000667.2:g.37154092_37154093insAGAG	GRCh38
NC_000005.9:g.37154194_37154195insAGAG , CM000667.1:g.37154194_37154195insAGAG	GRCh37
NC_000005.8:g.37189951_37189952insAGAG	NCBI36
NG_032772.1:g.100336_100337insCTCT
NG_032772.2:g.100336_100337insCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-100_1119-99insCTCT
ENST00000651892.2:c.8120-100_8120-99insCTCT MANE Select	ENSP00000498265.2:n.8120-100_8120-99insCTCT
ENST00000425232.6:c.7958-100_7958-99insCTCT	ENSP00000389014.2:n.7958-100_7958-99insCTCT
ENST00000508244.5:c.7958-100_7958-99insCTCT	ENSP00000421690.1:n.7958-100_7958-99insCTCT
ENST00000509849.5:c.5132-100_5132-99insCTCT	ENSP00000426337.1:n.5132-100_5132-99insCTCT
ENST00000509957.5:n.362-100_362-99insCTCT
ENST00000511210.5:n.411-100_411-99insCTCT
ENST00000511824.2:c.1234-100_1234-99insCTCT
ENST00000514429.5:c.5156-100_5156-99insCTCT	ENSP00000424223.1:n.5156-100_5156-99insCTCT
ENST00000515380.1:n.372-100_372-99insCTCT
NM_023073.3:c.7958-100_7958-99insCTCT	NP_075561.3:n.7958-100_7958-99insCTCT
XM_005248345.2:c.8120-100_8120-99insCTCT	XP_005248402.1:n.8120-100_8120-99insCTCT
XM_005248346.2:c.8117-100_8117-99insCTCT	XP_005248403.1:n.8117-100_8117-99insCTCT
XM_005248347.2:c.8117-100_8117-99insCTCT	XP_005248404.1:n.8117-100_8117-99insCTCT
XM_005248349.2:c.8009-100_8009-99insCTCT	XP_005248406.1:n.8009-100_8009-99insCTCT
XM_005248350.2:c.7991-100_7991-99insCTCT	XP_005248407.1:n.7991-100_7991-99insCTCT
XM_005248353.3:c.4763-100_4763-99insCTCT	XP_005248410.1:n.4763-100_4763-99insCTCT
XM_006714489.2:c.8120-100_8120-99insCTCT	XP_006714552.1:n.8120-100_8120-99insCTCT
XM_006714491.2:c.2693-100_2693-99insCTCT	XP_006714554.1:n.2693-100_2693-99insCTCT
XM_011514085.1:c.8120-100_8120-99insCTCT	XP_011512387.1:n.8120-100_8120-99insCTCT
XM_011514086.1:c.8120-100_8120-99insCTCT	XP_011512388.1:n.8120-100_8120-99insCTCT
XM_011514087.1:c.8066-100_8066-99insCTCT	XP_011512389.1:n.8066-100_8066-99insCTCT
XM_011514088.1:c.8012-100_8012-99insCTCT	XP_011512390.1:n.8012-100_8012-99insCTCT
XM_011514089.1:c.8120-100_8120-99insCTCT	XP_011512391.1:n.8120-100_8120-99insCTCT
XM_011514090.1:c.7802-100_7802-99insCTCT	XP_011512392.1:n.7802-100_7802-99insCTCT
XM_011514091.1:c.7448-100_7448-99insCTCT	XP_011512393.1:n.7448-100_7448-99insCTCT
XM_011514092.1:c.8120-100_8120-99insCTCT	XP_011512394.1:n.8120-100_8120-99insCTCT
XM_011514094.1:c.5345-100_5345-99insCTCT	XP_011512396.1:n.5345-100_5345-99insCTCT
XR_427661.2:n.8295-100_8295-99insCTCT
XR_925644.1:n.8295-100_8295-99insCTCT
XM_005248345.4:c.8120-100_8120-99insCTCT	XP_005248402.1:n.8120-100_8120-99insCTCT
XM_005248346.4:c.8117-100_8117-99insCTCT	XP_005248403.1:n.8117-100_8117-99insCTCT
XM_005248347.4:c.8117-100_8117-99insCTCT	XP_005248404.1:n.8117-100_8117-99insCTCT
XM_005248349.4:c.8009-100_8009-99insCTCT	XP_005248406.1:n.8009-100_8009-99insCTCT
XM_005248350.4:c.7991-100_7991-99insCTCT	XP_005248407.1:n.7991-100_7991-99insCTCT
XM_006714491.3:c.2693-100_2693-99insCTCT	XP_006714554.1:n.2693-100_2693-99insCTCT
XM_011514085.3:c.8120-100_8120-99insCTCT	XP_011512387.1:n.8120-100_8120-99insCTCT
XM_011514086.3:c.8120-100_8120-99insCTCT	XP_011512388.1:n.8120-100_8120-99insCTCT
XM_011514087.2:c.8066-100_8066-99insCTCT	XP_011512389.1:n.8066-100_8066-99insCTCT
XM_011514088.2:c.8012-100_8012-99insCTCT	XP_011512390.1:n.8012-100_8012-99insCTCT
XM_011514089.2:c.8120-100_8120-99insCTCT	XP_011512391.1:n.8120-100_8120-99insCTCT
XM_011514090.3:c.7802-100_7802-99insCTCT	XP_011512392.1:n.7802-100_7802-99insCTCT
XM_011514092.2:c.8120-100_8120-99insCTCT	XP_011512394.1:n.8120-100_8120-99insCTCT
XM_011514094.2:c.5345-100_5345-99insCTCT	XP_011512396.1:n.5345-100_5345-99insCTCT
XM_017009760.1:c.7931-100_7931-99insCTCT	XP_016865249.1:n.7931-100_7931-99insCTCT
XM_017009761.2:c.7931-100_7931-99insCTCT	XP_016865250.1:n.7931-100_7931-99insCTCT
XM_017009763.1:c.7127-100_7127-99insCTCT	XP_016865252.1:n.7127-100_7127-99insCTCT
XM_017009765.1:c.6932-100_6932-99insCTCT	XP_016865254.1:n.6932-100_6932-99insCTCT
XM_017009766.1:c.4763-100_4763-99insCTCT	XP_016865255.1:n.4763-100_4763-99insCTCT
XM_024446183.1:c.7931-100_7931-99insCTCT	XP_024301951.1:n.7931-100_7931-99insCTCT
XM_024446184.1:c.7802-100_7802-99insCTCT	XP_024301952.1:n.7802-100_7802-99insCTCT
XM_024446185.1:c.7448-100_7448-99insCTCT	XP_024301953.1:n.7448-100_7448-99insCTCT
XM_024446186.1:c.7127-100_7127-99insCTCT	XP_024301954.1:n.7127-100_7127-99insCTCT
XR_001742208.1:n.8289-100_8289-99insCTCT
XR_002956171.1:n.8235-100_8235-99insCTCT
XR_925644.2:n.8344-100_8344-99insCTCT
NM_001384732.1:c.8120-100_8120-99insCTCT MANE Select	NP_001371661.1:n.8120-100_8120-99insCTCT
NM_023073.4:c.7958-100_7958-99insCTCT	NP_075561.3:n.7958-100_7958-99insCTCT