Canonical Allele Identifier: CA2765914189

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154139_37154140insAC , CM000667.2:g.37154139_37154140insAC	GRCh38
NC_000005.9:g.37154241_37154242insAC , CM000667.1:g.37154241_37154242insAC	GRCh37
NC_000005.8:g.37189998_37189999insAC	NCBI36
NG_032772.1:g.100289_100290insGT
NG_032772.2:g.100289_100290insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-147_1119-146insGT
ENST00000651892.2:c.8120-147_8120-146insGT MANE Select	ENSP00000498265.2:n.8120-147_8120-146insGT
ENST00000425232.6:c.7958-147_7958-146insGT	ENSP00000389014.2:n.7958-147_7958-146insGT
ENST00000508244.5:c.7958-147_7958-146insGT	ENSP00000421690.1:n.7958-147_7958-146insGT
ENST00000509849.5:c.5132-147_5132-146insGT	ENSP00000426337.1:n.5132-147_5132-146insGT
ENST00000509957.5:n.362-147_362-146insGT
ENST00000511210.5:n.411-147_411-146insGT
ENST00000511824.2:c.1234-147_1234-146insGT
ENST00000514429.5:c.5156-147_5156-146insGT	ENSP00000424223.1:n.5156-147_5156-146insGT
ENST00000515380.1:n.372-147_372-146insGT
NM_023073.3:c.7958-147_7958-146insGT	NP_075561.3:n.7958-147_7958-146insGT
XM_005248345.2:c.8120-147_8120-146insGT	XP_005248402.1:n.8120-147_8120-146insGT
XM_005248346.2:c.8117-147_8117-146insGT	XP_005248403.1:n.8117-147_8117-146insGT
XM_005248347.2:c.8117-147_8117-146insGT	XP_005248404.1:n.8117-147_8117-146insGT
XM_005248349.2:c.8009-147_8009-146insGT	XP_005248406.1:n.8009-147_8009-146insGT
XM_005248350.2:c.7991-147_7991-146insGT	XP_005248407.1:n.7991-147_7991-146insGT
XM_005248353.3:c.4763-147_4763-146insGT	XP_005248410.1:n.4763-147_4763-146insGT
XM_006714489.2:c.8120-147_8120-146insGT	XP_006714552.1:n.8120-147_8120-146insGT
XM_006714491.2:c.2693-147_2693-146insGT	XP_006714554.1:n.2693-147_2693-146insGT
XM_011514085.1:c.8120-147_8120-146insGT	XP_011512387.1:n.8120-147_8120-146insGT
XM_011514086.1:c.8120-147_8120-146insGT	XP_011512388.1:n.8120-147_8120-146insGT
XM_011514087.1:c.8066-147_8066-146insGT	XP_011512389.1:n.8066-147_8066-146insGT
XM_011514088.1:c.8012-147_8012-146insGT	XP_011512390.1:n.8012-147_8012-146insGT
XM_011514089.1:c.8120-147_8120-146insGT	XP_011512391.1:n.8120-147_8120-146insGT
XM_011514090.1:c.7802-147_7802-146insGT	XP_011512392.1:n.7802-147_7802-146insGT
XM_011514091.1:c.7448-147_7448-146insGT	XP_011512393.1:n.7448-147_7448-146insGT
XM_011514092.1:c.8120-147_8120-146insGT	XP_011512394.1:n.8120-147_8120-146insGT
XM_011514094.1:c.5345-147_5345-146insGT	XP_011512396.1:n.5345-147_5345-146insGT
XR_427661.2:n.8295-147_8295-146insGT
XR_925644.1:n.8295-147_8295-146insGT
XM_005248345.4:c.8120-147_8120-146insGT	XP_005248402.1:n.8120-147_8120-146insGT
XM_005248346.4:c.8117-147_8117-146insGT	XP_005248403.1:n.8117-147_8117-146insGT
XM_005248347.4:c.8117-147_8117-146insGT	XP_005248404.1:n.8117-147_8117-146insGT
XM_005248349.4:c.8009-147_8009-146insGT	XP_005248406.1:n.8009-147_8009-146insGT
XM_005248350.4:c.7991-147_7991-146insGT	XP_005248407.1:n.7991-147_7991-146insGT
XM_006714491.3:c.2693-147_2693-146insGT	XP_006714554.1:n.2693-147_2693-146insGT
XM_011514085.3:c.8120-147_8120-146insGT	XP_011512387.1:n.8120-147_8120-146insGT
XM_011514086.3:c.8120-147_8120-146insGT	XP_011512388.1:n.8120-147_8120-146insGT
XM_011514087.2:c.8066-147_8066-146insGT	XP_011512389.1:n.8066-147_8066-146insGT
XM_011514088.2:c.8012-147_8012-146insGT	XP_011512390.1:n.8012-147_8012-146insGT
XM_011514089.2:c.8120-147_8120-146insGT	XP_011512391.1:n.8120-147_8120-146insGT
XM_011514090.3:c.7802-147_7802-146insGT	XP_011512392.1:n.7802-147_7802-146insGT
XM_011514092.2:c.8120-147_8120-146insGT	XP_011512394.1:n.8120-147_8120-146insGT
XM_011514094.2:c.5345-147_5345-146insGT	XP_011512396.1:n.5345-147_5345-146insGT
XM_017009760.1:c.7931-147_7931-146insGT	XP_016865249.1:n.7931-147_7931-146insGT
XM_017009761.2:c.7931-147_7931-146insGT	XP_016865250.1:n.7931-147_7931-146insGT
XM_017009763.1:c.7127-147_7127-146insGT	XP_016865252.1:n.7127-147_7127-146insGT
XM_017009765.1:c.6932-147_6932-146insGT	XP_016865254.1:n.6932-147_6932-146insGT
XM_017009766.1:c.4763-147_4763-146insGT	XP_016865255.1:n.4763-147_4763-146insGT
XM_024446183.1:c.7931-147_7931-146insGT	XP_024301951.1:n.7931-147_7931-146insGT
XM_024446184.1:c.7802-147_7802-146insGT	XP_024301952.1:n.7802-147_7802-146insGT
XM_024446185.1:c.7448-147_7448-146insGT	XP_024301953.1:n.7448-147_7448-146insGT
XM_024446186.1:c.7127-147_7127-146insGT	XP_024301954.1:n.7127-147_7127-146insGT
XR_001742208.1:n.8289-147_8289-146insGT
XR_002956171.1:n.8235-147_8235-146insGT
XR_925644.2:n.8344-147_8344-146insGT
NM_001384732.1:c.8120-147_8120-146insGT MANE Select	NP_001371661.1:n.8120-147_8120-146insGT
NM_023073.4:c.7958-147_7958-146insGT	NP_075561.3:n.7958-147_7958-146insGT