Canonical Allele Identifier: CA2544800279

Gene: PLEKHA7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.16895736_16895737insGAG , CM000673.2:g.16895736_16895737insGAG	GRCh38
NC_000011.9:g.16917283_16917284insGAG , CM000673.1:g.16917283_16917284insGAG	GRCh37
NC_000011.8:g.16873859_16873860insGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696749.1:c.92+17658_92+17659insCCT	ENSP00000512848.1:n.92+17658_92+17659insCCT
ENST00000698836.1:c.222-24553_222-24552insCCT	ENSP00000513972.1:n.222-24553_222-24552insCCT
ENST00000531066.6:c.222-24553_222-24552insCCT MANE Select	ENSP00000435389.1:n.222-24553_222-24552insCCT
ENST00000355661.7:c.222-24553_222-24552insCCT	ENSP00000347883.2:n.222-24553_222-24552insCCT
ENST00000529213.1:n.266-24553_266-24552insCCT
ENST00000531066.5:c.222-24553_222-24552insCCT	ENSP00000435389.1:n.222-24553_222-24552insCCT
ENST00000532079.1:c.82-105866_82-105865insCCT	ENSP00000434812.1:n.82-105866_82-105865insCCT
NM_175058.4:c.222-24553_222-24552insCCT	NP_778228.3:n.222-24553_222-24552insCCT
XM_006718149.2:c.222-24553_222-24552insCCT	XP_006718212.1:n.222-24553_222-24552insCCT
XM_011519910.1:c.84-24553_84-24552insCCT	XP_011518212.1:n.84-24553_84-24552insCCT
XM_011519912.1:c.18-24553_18-24552insCCT	XP_011518214.1:n.18-24553_18-24552insCCT
XM_011519913.1:c.168-24553_168-24552insCCT	XP_011518215.1:n.168-24553_168-24552insCCT
XM_011519914.1:c.222-24553_222-24552insCCT	XP_011518216.1:n.222-24553_222-24552insCCT
XM_011519916.1:c.168-24553_168-24552insCCT	XP_011518218.1:n.168-24553_168-24552insCCT
NM_001329630.1:c.222-24553_222-24552insCCT	NP_001316559.1:n.222-24553_222-24552insCCT
NM_001329631.1:c.222-24553_222-24552insCCT	NP_001316560.1:n.222-24553_222-24552insCCT
XM_017017241.2:c.222-24553_222-24552insCCT	XP_016872730.1:n.222-24553_222-24552insCCT
XM_017017242.2:c.222-24553_222-24552insCCT	XP_016872731.1:n.222-24553_222-24552insCCT
XM_024448356.1:c.222-24553_222-24552insCCT	XP_024304124.1:n.222-24553_222-24552insCCT
XM_024448357.1:c.222-24553_222-24552insCCT	XP_024304125.1:n.222-24553_222-24552insCCT
XM_024448358.1:c.222-24553_222-24552insCCT	XP_024304126.1:n.222-24553_222-24552insCCT
XM_024448359.1:c.222-24553_222-24552insCCT	XP_024304127.1:n.222-24553_222-24552insCCT
XM_024448360.1:c.222-24553_222-24552insCCT	XP_024304128.1:n.222-24553_222-24552insCCT
XM_024448361.1:c.84-24553_84-24552insCCT	XP_024304129.1:n.84-24553_84-24552insCCT
XM_024448363.1:c.222-24553_222-24552insCCT	XP_024304131.1:n.222-24553_222-24552insCCT
XM_024448364.1:c.222-24553_222-24552insCCT	XP_024304132.1:n.222-24553_222-24552insCCT
XM_024448368.1:c.-97-24553_-97-24552insCCT	XP_024304136.1:n.-97-24553_-97-24552insCCT
XM_024448370.1:c.222-24553_222-24552insCCT	XP_024304138.1:n.222-24553_222-24552insCCT
XR_002957126.1:n.244-24553_244-24552insCCT
NM_001329630.2:c.222-24553_222-24552insCCT MANE Select	NP_001316559.1:n.222-24553_222-24552insCCT
NM_001329631.2:c.222-24553_222-24552insCCT	NP_001316560.1:n.222-24553_222-24552insCCT
NM_175058.5:c.222-24553_222-24552insCCT	NP_778228.3:n.222-24553_222-24552insCCT