Canonical Allele Identifier: CA2765914107

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154026_37154027insAGA , CM000667.2:g.37154026_37154027insAGA	GRCh38
NC_000005.9:g.37154128_37154129insAGA , CM000667.1:g.37154128_37154129insAGA	GRCh37
NC_000005.8:g.37189885_37189886insAGA	NCBI36
NG_032772.1:g.100402_100403insTCT
NG_032772.2:g.100402_100403insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-34_1119-33insTCT
ENST00000651892.2:c.8120-34_8120-33insTCT MANE Select	ENSP00000498265.2:n.8120-34_8120-33insTCT
ENST00000425232.6:c.7958-34_7958-33insTCT	ENSP00000389014.2:n.7958-34_7958-33insTCT
ENST00000508244.5:c.7958-34_7958-33insTCT	ENSP00000421690.1:n.7958-34_7958-33insTCT
ENST00000509849.5:c.5132-34_5132-33insTCT	ENSP00000426337.1:n.5132-34_5132-33insTCT
ENST00000509957.5:n.362-34_362-33insTCT
ENST00000511210.5:n.411-34_411-33insTCT
ENST00000511824.2:c.1234-34_1234-33insTCT
ENST00000514429.5:c.5156-34_5156-33insTCT	ENSP00000424223.1:n.5156-34_5156-33insTCT
ENST00000515380.1:n.372-34_372-33insTCT
NM_023073.3:c.7958-34_7958-33insTCT	NP_075561.3:n.7958-34_7958-33insTCT
XM_005248345.2:c.8120-34_8120-33insTCT	XP_005248402.1:n.8120-34_8120-33insTCT
XM_005248346.2:c.8117-34_8117-33insTCT	XP_005248403.1:n.8117-34_8117-33insTCT
XM_005248347.2:c.8117-34_8117-33insTCT	XP_005248404.1:n.8117-34_8117-33insTCT
XM_005248349.2:c.8009-34_8009-33insTCT	XP_005248406.1:n.8009-34_8009-33insTCT
XM_005248350.2:c.7991-34_7991-33insTCT	XP_005248407.1:n.7991-34_7991-33insTCT
XM_005248353.3:c.4763-34_4763-33insTCT	XP_005248410.1:n.4763-34_4763-33insTCT
XM_006714489.2:c.8120-34_8120-33insTCT	XP_006714552.1:n.8120-34_8120-33insTCT
XM_006714491.2:c.2693-34_2693-33insTCT	XP_006714554.1:n.2693-34_2693-33insTCT
XM_011514085.1:c.8120-34_8120-33insTCT	XP_011512387.1:n.8120-34_8120-33insTCT
XM_011514086.1:c.8120-34_8120-33insTCT	XP_011512388.1:n.8120-34_8120-33insTCT
XM_011514087.1:c.8066-34_8066-33insTCT	XP_011512389.1:n.8066-34_8066-33insTCT
XM_011514088.1:c.8012-34_8012-33insTCT	XP_011512390.1:n.8012-34_8012-33insTCT
XM_011514089.1:c.8120-34_8120-33insTCT	XP_011512391.1:n.8120-34_8120-33insTCT
XM_011514090.1:c.7802-34_7802-33insTCT	XP_011512392.1:n.7802-34_7802-33insTCT
XM_011514091.1:c.7448-34_7448-33insTCT	XP_011512393.1:n.7448-34_7448-33insTCT
XM_011514092.1:c.8120-34_8120-33insTCT	XP_011512394.1:n.8120-34_8120-33insTCT
XM_011514094.1:c.5345-34_5345-33insTCT	XP_011512396.1:n.5345-34_5345-33insTCT
XR_427661.2:n.8295-34_8295-33insTCT
XR_925644.1:n.8295-34_8295-33insTCT
XM_005248345.4:c.8120-34_8120-33insTCT	XP_005248402.1:n.8120-34_8120-33insTCT
XM_005248346.4:c.8117-34_8117-33insTCT	XP_005248403.1:n.8117-34_8117-33insTCT
XM_005248347.4:c.8117-34_8117-33insTCT	XP_005248404.1:n.8117-34_8117-33insTCT
XM_005248349.4:c.8009-34_8009-33insTCT	XP_005248406.1:n.8009-34_8009-33insTCT
XM_005248350.4:c.7991-34_7991-33insTCT	XP_005248407.1:n.7991-34_7991-33insTCT
XM_006714491.3:c.2693-34_2693-33insTCT	XP_006714554.1:n.2693-34_2693-33insTCT
XM_011514085.3:c.8120-34_8120-33insTCT	XP_011512387.1:n.8120-34_8120-33insTCT
XM_011514086.3:c.8120-34_8120-33insTCT	XP_011512388.1:n.8120-34_8120-33insTCT
XM_011514087.2:c.8066-34_8066-33insTCT	XP_011512389.1:n.8066-34_8066-33insTCT
XM_011514088.2:c.8012-34_8012-33insTCT	XP_011512390.1:n.8012-34_8012-33insTCT
XM_011514089.2:c.8120-34_8120-33insTCT	XP_011512391.1:n.8120-34_8120-33insTCT
XM_011514090.3:c.7802-34_7802-33insTCT	XP_011512392.1:n.7802-34_7802-33insTCT
XM_011514092.2:c.8120-34_8120-33insTCT	XP_011512394.1:n.8120-34_8120-33insTCT
XM_011514094.2:c.5345-34_5345-33insTCT	XP_011512396.1:n.5345-34_5345-33insTCT
XM_017009760.1:c.7931-34_7931-33insTCT	XP_016865249.1:n.7931-34_7931-33insTCT
XM_017009761.2:c.7931-34_7931-33insTCT	XP_016865250.1:n.7931-34_7931-33insTCT
XM_017009763.1:c.7127-34_7127-33insTCT	XP_016865252.1:n.7127-34_7127-33insTCT
XM_017009765.1:c.6932-34_6932-33insTCT	XP_016865254.1:n.6932-34_6932-33insTCT
XM_017009766.1:c.4763-34_4763-33insTCT	XP_016865255.1:n.4763-34_4763-33insTCT
XM_024446183.1:c.7931-34_7931-33insTCT	XP_024301951.1:n.7931-34_7931-33insTCT
XM_024446184.1:c.7802-34_7802-33insTCT	XP_024301952.1:n.7802-34_7802-33insTCT
XM_024446185.1:c.7448-34_7448-33insTCT	XP_024301953.1:n.7448-34_7448-33insTCT
XM_024446186.1:c.7127-34_7127-33insTCT	XP_024301954.1:n.7127-34_7127-33insTCT
XR_001742208.1:n.8289-34_8289-33insTCT
XR_002956171.1:n.8235-34_8235-33insTCT
XR_925644.2:n.8344-34_8344-33insTCT
NM_001384732.1:c.8120-34_8120-33insTCT MANE Select	NP_001371661.1:n.8120-34_8120-33insTCT
NM_023073.4:c.7958-34_7958-33insTCT	NP_075561.3:n.7958-34_7958-33insTCT