Canonical Allele Identifier: CA2765914161

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154104_37154105insG , CM000667.2:g.37154104_37154105insG	GRCh38
NC_000005.9:g.37154206_37154207insG , CM000667.1:g.37154206_37154207insG	GRCh37
NC_000005.8:g.37189963_37189964insG	NCBI36
NG_032772.1:g.100324_100325insC
NG_032772.2:g.100324_100325insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-112_1119-111insC
ENST00000651892.2:c.8120-112_8120-111insC MANE Select	ENSP00000498265.2:n.8120-112_8120-111insC
ENST00000425232.6:c.7958-112_7958-111insC	ENSP00000389014.2:n.7958-112_7958-111insC
ENST00000508244.5:c.7958-112_7958-111insC	ENSP00000421690.1:n.7958-112_7958-111insC
ENST00000509849.5:c.5132-112_5132-111insC	ENSP00000426337.1:n.5132-112_5132-111insC
ENST00000509957.5:n.362-112_362-111insC
ENST00000511210.5:n.411-112_411-111insC
ENST00000511824.2:c.1234-112_1234-111insC
ENST00000514429.5:c.5156-112_5156-111insC	ENSP00000424223.1:n.5156-112_5156-111insC
ENST00000515380.1:n.372-112_372-111insC
NM_023073.3:c.7958-112_7958-111insC	NP_075561.3:n.7958-112_7958-111insC
XM_005248345.2:c.8120-112_8120-111insC	XP_005248402.1:n.8120-112_8120-111insC
XM_005248346.2:c.8117-112_8117-111insC	XP_005248403.1:n.8117-112_8117-111insC
XM_005248347.2:c.8117-112_8117-111insC	XP_005248404.1:n.8117-112_8117-111insC
XM_005248349.2:c.8009-112_8009-111insC	XP_005248406.1:n.8009-112_8009-111insC
XM_005248350.2:c.7991-112_7991-111insC	XP_005248407.1:n.7991-112_7991-111insC
XM_005248353.3:c.4763-112_4763-111insC	XP_005248410.1:n.4763-112_4763-111insC
XM_006714489.2:c.8120-112_8120-111insC	XP_006714552.1:n.8120-112_8120-111insC
XM_006714491.2:c.2693-112_2693-111insC	XP_006714554.1:n.2693-112_2693-111insC
XM_011514085.1:c.8120-112_8120-111insC	XP_011512387.1:n.8120-112_8120-111insC
XM_011514086.1:c.8120-112_8120-111insC	XP_011512388.1:n.8120-112_8120-111insC
XM_011514087.1:c.8066-112_8066-111insC	XP_011512389.1:n.8066-112_8066-111insC
XM_011514088.1:c.8012-112_8012-111insC	XP_011512390.1:n.8012-112_8012-111insC
XM_011514089.1:c.8120-112_8120-111insC	XP_011512391.1:n.8120-112_8120-111insC
XM_011514090.1:c.7802-112_7802-111insC	XP_011512392.1:n.7802-112_7802-111insC
XM_011514091.1:c.7448-112_7448-111insC	XP_011512393.1:n.7448-112_7448-111insC
XM_011514092.1:c.8120-112_8120-111insC	XP_011512394.1:n.8120-112_8120-111insC
XM_011514094.1:c.5345-112_5345-111insC	XP_011512396.1:n.5345-112_5345-111insC
XR_427661.2:n.8295-112_8295-111insC
XR_925644.1:n.8295-112_8295-111insC
XM_005248345.4:c.8120-112_8120-111insC	XP_005248402.1:n.8120-112_8120-111insC
XM_005248346.4:c.8117-112_8117-111insC	XP_005248403.1:n.8117-112_8117-111insC
XM_005248347.4:c.8117-112_8117-111insC	XP_005248404.1:n.8117-112_8117-111insC
XM_005248349.4:c.8009-112_8009-111insC	XP_005248406.1:n.8009-112_8009-111insC
XM_005248350.4:c.7991-112_7991-111insC	XP_005248407.1:n.7991-112_7991-111insC
XM_006714491.3:c.2693-112_2693-111insC	XP_006714554.1:n.2693-112_2693-111insC
XM_011514085.3:c.8120-112_8120-111insC	XP_011512387.1:n.8120-112_8120-111insC
XM_011514086.3:c.8120-112_8120-111insC	XP_011512388.1:n.8120-112_8120-111insC
XM_011514087.2:c.8066-112_8066-111insC	XP_011512389.1:n.8066-112_8066-111insC
XM_011514088.2:c.8012-112_8012-111insC	XP_011512390.1:n.8012-112_8012-111insC
XM_011514089.2:c.8120-112_8120-111insC	XP_011512391.1:n.8120-112_8120-111insC
XM_011514090.3:c.7802-112_7802-111insC	XP_011512392.1:n.7802-112_7802-111insC
XM_011514092.2:c.8120-112_8120-111insC	XP_011512394.1:n.8120-112_8120-111insC
XM_011514094.2:c.5345-112_5345-111insC	XP_011512396.1:n.5345-112_5345-111insC
XM_017009760.1:c.7931-112_7931-111insC	XP_016865249.1:n.7931-112_7931-111insC
XM_017009761.2:c.7931-112_7931-111insC	XP_016865250.1:n.7931-112_7931-111insC
XM_017009763.1:c.7127-112_7127-111insC	XP_016865252.1:n.7127-112_7127-111insC
XM_017009765.1:c.6932-112_6932-111insC	XP_016865254.1:n.6932-112_6932-111insC
XM_017009766.1:c.4763-112_4763-111insC	XP_016865255.1:n.4763-112_4763-111insC
XM_024446183.1:c.7931-112_7931-111insC	XP_024301951.1:n.7931-112_7931-111insC
XM_024446184.1:c.7802-112_7802-111insC	XP_024301952.1:n.7802-112_7802-111insC
XM_024446185.1:c.7448-112_7448-111insC	XP_024301953.1:n.7448-112_7448-111insC
XM_024446186.1:c.7127-112_7127-111insC	XP_024301954.1:n.7127-112_7127-111insC
XR_001742208.1:n.8289-112_8289-111insC
XR_002956171.1:n.8235-112_8235-111insC
XR_925644.2:n.8344-112_8344-111insC
NM_001384732.1:c.8120-112_8120-111insC MANE Select	NP_001371661.1:n.8120-112_8120-111insC
NM_023073.4:c.7958-112_7958-111insC	NP_075561.3:n.7958-112_7958-111insC