Canonical Allele Identifier: CA2765914103

Gene: CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37154001_37154003del , CM000667.2:g.37154001_37154003del	GRCh38
NC_000005.9:g.37154103_37154105del , CM000667.1:g.37154103_37154105del	GRCh37
NC_000005.8:g.37189860_37189862del	NCBI36
NG_032772.1:g.100428_100430del
NG_032772.2:g.100428_100430del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510830.2:n.1119-8_1119-6del
ENST00000651892.2:c.8120-8_8120-6del MANE Select	ENSP00000498265.2:n.8120-8_8120-6del
ENST00000425232.6:c.7958-8_7958-6del	ENSP00000389014.2:n.7958-8_7958-6del
ENST00000508244.5:c.7958-8_7958-6del	ENSP00000421690.1:n.7958-8_7958-6del
ENST00000509849.5:c.5132-8_5132-6del	ENSP00000426337.1:n.5132-8_5132-6del
ENST00000509957.5:n.362-8_362-6del
ENST00000511210.5:n.411-8_411-6del
ENST00000511824.2:c.1234-8_1234-6del
ENST00000514429.5:c.5156-8_5156-6del	ENSP00000424223.1:n.5156-8_5156-6del
ENST00000515380.1:n.372-8_372-6del
NM_023073.3:c.7958-8_7958-6del	NP_075561.3:n.7958-8_7958-6del
XM_005248345.2:c.8120-8_8120-6del	XP_005248402.1:n.8120-8_8120-6del
XM_005248346.2:c.8117-8_8117-6del	XP_005248403.1:n.8117-8_8117-6del
XM_005248347.2:c.8117-8_8117-6del	XP_005248404.1:n.8117-8_8117-6del
XM_005248349.2:c.8009-8_8009-6del	XP_005248406.1:n.8009-8_8009-6del
XM_005248350.2:c.7991-8_7991-6del	XP_005248407.1:n.7991-8_7991-6del
XM_005248353.3:c.4763-8_4763-6del	XP_005248410.1:n.4763-8_4763-6del
XM_006714489.2:c.8120-8_8120-6del	XP_006714552.1:n.8120-8_8120-6del
XM_006714491.2:c.2693-8_2693-6del	XP_006714554.1:n.2693-8_2693-6del
XM_011514085.1:c.8120-8_8120-6del	XP_011512387.1:n.8120-8_8120-6del
XM_011514086.1:c.8120-8_8120-6del	XP_011512388.1:n.8120-8_8120-6del
XM_011514087.1:c.8066-8_8066-6del	XP_011512389.1:n.8066-8_8066-6del
XM_011514088.1:c.8012-8_8012-6del	XP_011512390.1:n.8012-8_8012-6del
XM_011514089.1:c.8120-8_8120-6del	XP_011512391.1:n.8120-8_8120-6del
XM_011514090.1:c.7802-8_7802-6del	XP_011512392.1:n.7802-8_7802-6del
XM_011514091.1:c.7448-8_7448-6del	XP_011512393.1:n.7448-8_7448-6del
XM_011514092.1:c.8120-8_8120-6del	XP_011512394.1:n.8120-8_8120-6del
XM_011514094.1:c.5345-8_5345-6del	XP_011512396.1:n.5345-8_5345-6del
XR_427661.2:n.8295-8_8295-6del
XR_925644.1:n.8295-8_8295-6del
XM_005248345.4:c.8120-8_8120-6del	XP_005248402.1:n.8120-8_8120-6del
XM_005248346.4:c.8117-8_8117-6del	XP_005248403.1:n.8117-8_8117-6del
XM_005248347.4:c.8117-8_8117-6del	XP_005248404.1:n.8117-8_8117-6del
XM_005248349.4:c.8009-8_8009-6del	XP_005248406.1:n.8009-8_8009-6del
XM_005248350.4:c.7991-8_7991-6del	XP_005248407.1:n.7991-8_7991-6del
XM_006714491.3:c.2693-8_2693-6del	XP_006714554.1:n.2693-8_2693-6del
XM_011514085.3:c.8120-8_8120-6del	XP_011512387.1:n.8120-8_8120-6del
XM_011514086.3:c.8120-8_8120-6del	XP_011512388.1:n.8120-8_8120-6del
XM_011514087.2:c.8066-8_8066-6del	XP_011512389.1:n.8066-8_8066-6del
XM_011514088.2:c.8012-8_8012-6del	XP_011512390.1:n.8012-8_8012-6del
XM_011514089.2:c.8120-8_8120-6del	XP_011512391.1:n.8120-8_8120-6del
XM_011514090.3:c.7802-8_7802-6del	XP_011512392.1:n.7802-8_7802-6del
XM_011514092.2:c.8120-8_8120-6del	XP_011512394.1:n.8120-8_8120-6del
XM_011514094.2:c.5345-8_5345-6del	XP_011512396.1:n.5345-8_5345-6del
XM_017009760.1:c.7931-8_7931-6del	XP_016865249.1:n.7931-8_7931-6del
XM_017009761.2:c.7931-8_7931-6del	XP_016865250.1:n.7931-8_7931-6del
XM_017009763.1:c.7127-8_7127-6del	XP_016865252.1:n.7127-8_7127-6del
XM_017009765.1:c.6932-8_6932-6del	XP_016865254.1:n.6932-8_6932-6del
XM_017009766.1:c.4763-8_4763-6del	XP_016865255.1:n.4763-8_4763-6del
XM_024446183.1:c.7931-8_7931-6del	XP_024301951.1:n.7931-8_7931-6del
XM_024446184.1:c.7802-8_7802-6del	XP_024301952.1:n.7802-8_7802-6del
XM_024446185.1:c.7448-8_7448-6del	XP_024301953.1:n.7448-8_7448-6del
XM_024446186.1:c.7127-8_7127-6del	XP_024301954.1:n.7127-8_7127-6del
XR_001742208.1:n.8289-8_8289-6del
XR_002956171.1:n.8235-8_8235-6del
XR_925644.2:n.8344-8_8344-6del
NM_001384732.1:c.8120-8_8120-6del MANE Select	NP_001371661.1:n.8120-8_8120-6del
NM_023073.4:c.7958-8_7958-6del	NP_075561.3:n.7958-8_7958-6del