Canonical Allele Identifier: CA2765914122

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154049_37154050insAC , CM000667.2:g.37154049_37154050insAC	GRCh38
NC_000005.9:g.37154151_37154152insAC , CM000667.1:g.37154151_37154152insAC	GRCh37
NC_000005.8:g.37189908_37189909insAC	NCBI36
NG_032772.1:g.100379_100380insGT
NG_032772.2:g.100379_100380insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-57_1119-56insGT
ENST00000651892.2:c.8120-57_8120-56insGT MANE Select	ENSP00000498265.2:n.8120-57_8120-56insGT
ENST00000425232.6:c.7958-57_7958-56insGT	ENSP00000389014.2:n.7958-57_7958-56insGT
ENST00000508244.5:c.7958-57_7958-56insGT	ENSP00000421690.1:n.7958-57_7958-56insGT
ENST00000509849.5:c.5132-57_5132-56insGT	ENSP00000426337.1:n.5132-57_5132-56insGT
ENST00000509957.5:n.362-57_362-56insGT
ENST00000511210.5:n.411-57_411-56insGT
ENST00000511824.2:c.1234-57_1234-56insGT
ENST00000514429.5:c.5156-57_5156-56insGT	ENSP00000424223.1:n.5156-57_5156-56insGT
ENST00000515380.1:n.372-57_372-56insGT
NM_023073.3:c.7958-57_7958-56insGT	NP_075561.3:n.7958-57_7958-56insGT
XM_005248345.2:c.8120-57_8120-56insGT	XP_005248402.1:n.8120-57_8120-56insGT
XM_005248346.2:c.8117-57_8117-56insGT	XP_005248403.1:n.8117-57_8117-56insGT
XM_005248347.2:c.8117-57_8117-56insGT	XP_005248404.1:n.8117-57_8117-56insGT
XM_005248349.2:c.8009-57_8009-56insGT	XP_005248406.1:n.8009-57_8009-56insGT
XM_005248350.2:c.7991-57_7991-56insGT	XP_005248407.1:n.7991-57_7991-56insGT
XM_005248353.3:c.4763-57_4763-56insGT	XP_005248410.1:n.4763-57_4763-56insGT
XM_006714489.2:c.8120-57_8120-56insGT	XP_006714552.1:n.8120-57_8120-56insGT
XM_006714491.2:c.2693-57_2693-56insGT	XP_006714554.1:n.2693-57_2693-56insGT
XM_011514085.1:c.8120-57_8120-56insGT	XP_011512387.1:n.8120-57_8120-56insGT
XM_011514086.1:c.8120-57_8120-56insGT	XP_011512388.1:n.8120-57_8120-56insGT
XM_011514087.1:c.8066-57_8066-56insGT	XP_011512389.1:n.8066-57_8066-56insGT
XM_011514088.1:c.8012-57_8012-56insGT	XP_011512390.1:n.8012-57_8012-56insGT
XM_011514089.1:c.8120-57_8120-56insGT	XP_011512391.1:n.8120-57_8120-56insGT
XM_011514090.1:c.7802-57_7802-56insGT	XP_011512392.1:n.7802-57_7802-56insGT
XM_011514091.1:c.7448-57_7448-56insGT	XP_011512393.1:n.7448-57_7448-56insGT
XM_011514092.1:c.8120-57_8120-56insGT	XP_011512394.1:n.8120-57_8120-56insGT
XM_011514094.1:c.5345-57_5345-56insGT	XP_011512396.1:n.5345-57_5345-56insGT
XR_427661.2:n.8295-57_8295-56insGT
XR_925644.1:n.8295-57_8295-56insGT
XM_005248345.4:c.8120-57_8120-56insGT	XP_005248402.1:n.8120-57_8120-56insGT
XM_005248346.4:c.8117-57_8117-56insGT	XP_005248403.1:n.8117-57_8117-56insGT
XM_005248347.4:c.8117-57_8117-56insGT	XP_005248404.1:n.8117-57_8117-56insGT
XM_005248349.4:c.8009-57_8009-56insGT	XP_005248406.1:n.8009-57_8009-56insGT
XM_005248350.4:c.7991-57_7991-56insGT	XP_005248407.1:n.7991-57_7991-56insGT
XM_006714491.3:c.2693-57_2693-56insGT	XP_006714554.1:n.2693-57_2693-56insGT
XM_011514085.3:c.8120-57_8120-56insGT	XP_011512387.1:n.8120-57_8120-56insGT
XM_011514086.3:c.8120-57_8120-56insGT	XP_011512388.1:n.8120-57_8120-56insGT
XM_011514087.2:c.8066-57_8066-56insGT	XP_011512389.1:n.8066-57_8066-56insGT
XM_011514088.2:c.8012-57_8012-56insGT	XP_011512390.1:n.8012-57_8012-56insGT
XM_011514089.2:c.8120-57_8120-56insGT	XP_011512391.1:n.8120-57_8120-56insGT
XM_011514090.3:c.7802-57_7802-56insGT	XP_011512392.1:n.7802-57_7802-56insGT
XM_011514092.2:c.8120-57_8120-56insGT	XP_011512394.1:n.8120-57_8120-56insGT
XM_011514094.2:c.5345-57_5345-56insGT	XP_011512396.1:n.5345-57_5345-56insGT
XM_017009760.1:c.7931-57_7931-56insGT	XP_016865249.1:n.7931-57_7931-56insGT
XM_017009761.2:c.7931-57_7931-56insGT	XP_016865250.1:n.7931-57_7931-56insGT
XM_017009763.1:c.7127-57_7127-56insGT	XP_016865252.1:n.7127-57_7127-56insGT
XM_017009765.1:c.6932-57_6932-56insGT	XP_016865254.1:n.6932-57_6932-56insGT
XM_017009766.1:c.4763-57_4763-56insGT	XP_016865255.1:n.4763-57_4763-56insGT
XM_024446183.1:c.7931-57_7931-56insGT	XP_024301951.1:n.7931-57_7931-56insGT
XM_024446184.1:c.7802-57_7802-56insGT	XP_024301952.1:n.7802-57_7802-56insGT
XM_024446185.1:c.7448-57_7448-56insGT	XP_024301953.1:n.7448-57_7448-56insGT
XM_024446186.1:c.7127-57_7127-56insGT	XP_024301954.1:n.7127-57_7127-56insGT
XR_001742208.1:n.8289-57_8289-56insGT
XR_002956171.1:n.8235-57_8235-56insGT
XR_925644.2:n.8344-57_8344-56insGT
NM_001384732.1:c.8120-57_8120-56insGT MANE Select	NP_001371661.1:n.8120-57_8120-56insGT
NM_023073.4:c.7958-57_7958-56insGT	NP_075561.3:n.7958-57_7958-56insGT