Canonical Allele Identifier: CA2765914191

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154140_37154141insAG , CM000667.2:g.37154140_37154141insAG	GRCh38
NC_000005.9:g.37154242_37154243insAG , CM000667.1:g.37154242_37154243insAG	GRCh37
NC_000005.8:g.37189999_37190000insAG	NCBI36
NG_032772.1:g.100288_100289insCT
NG_032772.2:g.100288_100289insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-148_1119-147insCT
ENST00000651892.2:c.8120-148_8120-147insCT MANE Select	ENSP00000498265.2:n.8120-148_8120-147insCT
ENST00000425232.6:c.7958-148_7958-147insCT	ENSP00000389014.2:n.7958-148_7958-147insCT
ENST00000508244.5:c.7958-148_7958-147insCT	ENSP00000421690.1:n.7958-148_7958-147insCT
ENST00000509849.5:c.5132-148_5132-147insCT	ENSP00000426337.1:n.5132-148_5132-147insCT
ENST00000509957.5:n.362-148_362-147insCT
ENST00000511210.5:n.411-148_411-147insCT
ENST00000511824.2:c.1234-148_1234-147insCT
ENST00000514429.5:c.5156-148_5156-147insCT	ENSP00000424223.1:n.5156-148_5156-147insCT
ENST00000515380.1:n.372-148_372-147insCT
NM_023073.3:c.7958-148_7958-147insCT	NP_075561.3:n.7958-148_7958-147insCT
XM_005248345.2:c.8120-148_8120-147insCT	XP_005248402.1:n.8120-148_8120-147insCT
XM_005248346.2:c.8117-148_8117-147insCT	XP_005248403.1:n.8117-148_8117-147insCT
XM_005248347.2:c.8117-148_8117-147insCT	XP_005248404.1:n.8117-148_8117-147insCT
XM_005248349.2:c.8009-148_8009-147insCT	XP_005248406.1:n.8009-148_8009-147insCT
XM_005248350.2:c.7991-148_7991-147insCT	XP_005248407.1:n.7991-148_7991-147insCT
XM_005248353.3:c.4763-148_4763-147insCT	XP_005248410.1:n.4763-148_4763-147insCT
XM_006714489.2:c.8120-148_8120-147insCT	XP_006714552.1:n.8120-148_8120-147insCT
XM_006714491.2:c.2693-148_2693-147insCT	XP_006714554.1:n.2693-148_2693-147insCT
XM_011514085.1:c.8120-148_8120-147insCT	XP_011512387.1:n.8120-148_8120-147insCT
XM_011514086.1:c.8120-148_8120-147insCT	XP_011512388.1:n.8120-148_8120-147insCT
XM_011514087.1:c.8066-148_8066-147insCT	XP_011512389.1:n.8066-148_8066-147insCT
XM_011514088.1:c.8012-148_8012-147insCT	XP_011512390.1:n.8012-148_8012-147insCT
XM_011514089.1:c.8120-148_8120-147insCT	XP_011512391.1:n.8120-148_8120-147insCT
XM_011514090.1:c.7802-148_7802-147insCT	XP_011512392.1:n.7802-148_7802-147insCT
XM_011514091.1:c.7448-148_7448-147insCT	XP_011512393.1:n.7448-148_7448-147insCT
XM_011514092.1:c.8120-148_8120-147insCT	XP_011512394.1:n.8120-148_8120-147insCT
XM_011514094.1:c.5345-148_5345-147insCT	XP_011512396.1:n.5345-148_5345-147insCT
XR_427661.2:n.8295-148_8295-147insCT
XR_925644.1:n.8295-148_8295-147insCT
XM_005248345.4:c.8120-148_8120-147insCT	XP_005248402.1:n.8120-148_8120-147insCT
XM_005248346.4:c.8117-148_8117-147insCT	XP_005248403.1:n.8117-148_8117-147insCT
XM_005248347.4:c.8117-148_8117-147insCT	XP_005248404.1:n.8117-148_8117-147insCT
XM_005248349.4:c.8009-148_8009-147insCT	XP_005248406.1:n.8009-148_8009-147insCT
XM_005248350.4:c.7991-148_7991-147insCT	XP_005248407.1:n.7991-148_7991-147insCT
XM_006714491.3:c.2693-148_2693-147insCT	XP_006714554.1:n.2693-148_2693-147insCT
XM_011514085.3:c.8120-148_8120-147insCT	XP_011512387.1:n.8120-148_8120-147insCT
XM_011514086.3:c.8120-148_8120-147insCT	XP_011512388.1:n.8120-148_8120-147insCT
XM_011514087.2:c.8066-148_8066-147insCT	XP_011512389.1:n.8066-148_8066-147insCT
XM_011514088.2:c.8012-148_8012-147insCT	XP_011512390.1:n.8012-148_8012-147insCT
XM_011514089.2:c.8120-148_8120-147insCT	XP_011512391.1:n.8120-148_8120-147insCT
XM_011514090.3:c.7802-148_7802-147insCT	XP_011512392.1:n.7802-148_7802-147insCT
XM_011514092.2:c.8120-148_8120-147insCT	XP_011512394.1:n.8120-148_8120-147insCT
XM_011514094.2:c.5345-148_5345-147insCT	XP_011512396.1:n.5345-148_5345-147insCT
XM_017009760.1:c.7931-148_7931-147insCT	XP_016865249.1:n.7931-148_7931-147insCT
XM_017009761.2:c.7931-148_7931-147insCT	XP_016865250.1:n.7931-148_7931-147insCT
XM_017009763.1:c.7127-148_7127-147insCT	XP_016865252.1:n.7127-148_7127-147insCT
XM_017009765.1:c.6932-148_6932-147insCT	XP_016865254.1:n.6932-148_6932-147insCT
XM_017009766.1:c.4763-148_4763-147insCT	XP_016865255.1:n.4763-148_4763-147insCT
XM_024446183.1:c.7931-148_7931-147insCT	XP_024301951.1:n.7931-148_7931-147insCT
XM_024446184.1:c.7802-148_7802-147insCT	XP_024301952.1:n.7802-148_7802-147insCT
XM_024446185.1:c.7448-148_7448-147insCT	XP_024301953.1:n.7448-148_7448-147insCT
XM_024446186.1:c.7127-148_7127-147insCT	XP_024301954.1:n.7127-148_7127-147insCT
XR_001742208.1:n.8289-148_8289-147insCT
XR_002956171.1:n.8235-148_8235-147insCT
XR_925644.2:n.8344-148_8344-147insCT
NM_001384732.1:c.8120-148_8120-147insCT MANE Select	NP_001371661.1:n.8120-148_8120-147insCT
NM_023073.4:c.7958-148_7958-147insCT	NP_075561.3:n.7958-148_7958-147insCT