Canonical Allele Identifier: CA1697520546

Gene: PLEKHA8

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30043465_30043469delinsGCCAT , CM000669.2:g.30043465_30043469delinsGCCAT	GRCh38
NC_000007.13:g.30083081_30083085delinsGCCAT , CM000669.1:g.30083081_30083085delinsGCCAT	GRCh37
NC_000007.12:g.30049606_30049610delinsGCCAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707142.1:n.32-1620_32-1616delinsGCCAT
ENST00000440706.3:c.41-1620_41-1616delinsGCCAT	ENSP00000407802.2:n.41-1620_41-1616delinsGCCAT
ENST00000449726.6:c.41-1620_41-1616delinsGCCAT MANE Select	ENSP00000397947.1:n.41-1620_41-1616delinsGCCAT
ENST00000649443.1:c.*17-1620_*17-1616delinsGCCAT	ENSP00000497449.1:n.*17-1620_*17-1616delinsGCCAT
ENST00000258679.11:c.41-1620_41-1616delinsGCCAT	ENSP00000258679.7:n.41-1620_41-1616delinsGCCAT
ENST00000396257.6:c.41-1620_41-1616delinsGCCAT	ENSP00000379556.2:n.41-1620_41-1616delinsGCCAT
ENST00000396259.5:c.41-1620_41-1616delinsGCCAT	ENSP00000379558.1:n.41-1620_41-1616delinsGCCAT
ENST00000440706.2:c.119-1620_119-1616delinsGCCAT	ENSP00000407802.1:n.119-1620_119-1616delinsGCCAT
ENST00000449726.5:c.41-1620_41-1616delinsGCCAT	ENSP00000397947.1:n.41-1620_41-1616delinsGCCAT
ENST00000483799.5:n.145-1620_145-1616delinsGCCAT
ENST00000622102.4:c.41-1620_41-1616delinsGCCAT	ENSP00000484427.1:n.41-1620_41-1616delinsGCCAT
NM_001197026.1:c.41-1620_41-1616delinsGCCAT	NP_001183955.1:n.41-1620_41-1616delinsGCCAT
NM_001197027.1:c.41-1620_41-1616delinsGCCAT	NP_001183956.1:n.41-1620_41-1616delinsGCCAT
NM_032639.3:c.41-1620_41-1616delinsGCCAT	NP_116028.1:n.41-1620_41-1616delinsGCCAT
XM_005249897.2:c.41-1620_41-1616delinsGCCAT	XP_005249954.1:n.41-1620_41-1616delinsGCCAT
XM_005249898.1:c.-480-1620_-480-1616delinsGCCAT	XP_005249955.1:n.-480-1620_-480-1616delinsGCCAT
XM_011515591.1:c.41-1620_41-1616delinsGCCAT	XP_011513893.1:n.41-1620_41-1616delinsGCCAT
XM_011515592.1:c.41-1620_41-1616delinsGCCAT	XP_011513894.1:n.41-1620_41-1616delinsGCCAT
XM_011515593.1:c.41-1620_41-1616delinsGCCAT	XP_011513895.1:n.41-1620_41-1616delinsGCCAT
XM_011515594.1:c.41-1620_41-1616delinsGCCAT	XP_011513896.1:n.41-1620_41-1616delinsGCCAT
XM_011515595.1:c.41-1620_41-1616delinsGCCAT	XP_011513897.1:n.41-1620_41-1616delinsGCCAT
NM_001350973.1:c.41-1620_41-1616delinsGCCAT	NP_001337902.1:n.41-1620_41-1616delinsGCCAT
NM_001350974.1:c.41-1620_41-1616delinsGCCAT	NP_001337903.1:n.41-1620_41-1616delinsGCCAT
NM_001350975.1:c.-616-1620_-616-1616delinsGCCAT	NP_001337904.1:n.-616-1620_-616-1616delinsGCCAT
NM_001363473.1:c.41-1620_41-1616delinsGCCAT	NP_001350402.1:n.41-1620_41-1616delinsGCCAT
XM_011515591.2:c.41-1620_41-1616delinsGCCAT	XP_011513893.1:n.41-1620_41-1616delinsGCCAT
XM_011515592.3:c.41-1620_41-1616delinsGCCAT	XP_011513894.1:n.41-1620_41-1616delinsGCCAT
XM_017012744.1:c.41-1620_41-1616delinsGCCAT	XP_016868233.1:n.41-1620_41-1616delinsGCCAT
XM_017012746.1:c.-616-1620_-616-1616delinsGCCAT	XP_016868235.1:n.-616-1620_-616-1616delinsGCCAT
XM_017012747.1:c.-649-1620_-649-1616delinsGCCAT	XP_016868236.1:n.-649-1620_-649-1616delinsGCCAT
NM_001197026.2:c.41-1620_41-1616delinsGCCAT MANE Select	NP_001183955.1:n.41-1620_41-1616delinsGCCAT
NM_001350973.2:c.41-1620_41-1616delinsGCCAT	NP_001337902.1:n.41-1620_41-1616delinsGCCAT
NM_001350974.2:c.41-1620_41-1616delinsGCCAT	NP_001337903.1:n.41-1620_41-1616delinsGCCAT
NM_032639.4:c.41-1620_41-1616delinsGCCAT	NP_116028.1:n.41-1620_41-1616delinsGCCAT
NM_001197027.2:c.41-1620_41-1616delinsGCCAT	NP_001183956.1:n.41-1620_41-1616delinsGCCAT
NM_001350975.2:c.-616-1620_-616-1616delinsGCCAT	NP_001337904.1:n.-616-1620_-616-1616delinsGCCAT