Canonical Allele Identifier: CA1954881296

Gene: PLEKHA7

Linked Data

• dbSNP Id: rs1853837920

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.16860310_16860327del , CM000673.2:g.16860310_16860327del	GRCh38
NC_000011.9:g.16881857_16881874del , CM000673.1:g.16881857_16881874del	GRCh37
NC_000011.8:g.16838433_16838450del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696749.1:c.177-4411_177-4394del	ENSP00000512848.1:n.177-4411_177-4394del
ENST00000698836.1:c.306-4411_306-4394del	ENSP00000513972.1:n.306-4411_306-4394del
ENST00000531066.6:c.306-4411_306-4394del MANE Select	ENSP00000435389.1:n.306-4411_306-4394del
ENST00000355661.7:c.306-4411_306-4394del	ENSP00000347883.2:n.306-4411_306-4394del
ENST00000528376.5:c.-13-4411_-13-4394del	ENSP00000435806.1:n.-13-4411_-13-4394del
ENST00000528637.5:n.421-4411_421-4394del
ENST00000529213.1:n.350-4411_350-4394del
ENST00000531066.5:c.306-4411_306-4394del	ENSP00000435389.1:n.306-4411_306-4394del
ENST00000532079.1:c.82-70456_82-70439del	ENSP00000434812.1:n.82-70456_82-70439del
NM_175058.4:c.306-4411_306-4394del	NP_778228.3:n.306-4411_306-4394del
XM_006718149.2:c.306-4411_306-4394del	XP_006718212.1:n.306-4411_306-4394del
XM_011519910.1:c.168-4411_168-4394del	XP_011518212.1:n.168-4411_168-4394del
XM_011519911.1:c.132-4411_132-4394del	XP_011518213.1:n.132-4411_132-4394del
XM_011519912.1:c.102-4411_102-4394del	XP_011518214.1:n.102-4411_102-4394del
XM_011519913.1:c.252-4411_252-4394del	XP_011518215.1:n.252-4411_252-4394del
XM_011519914.1:c.306-4411_306-4394del	XP_011518216.1:n.306-4411_306-4394del
XM_011519916.1:c.252-4411_252-4394del	XP_011518218.1:n.252-4411_252-4394del
NM_001329630.1:c.306-4411_306-4394del	NP_001316559.1:n.306-4411_306-4394del
NM_001329631.1:c.306-4411_306-4394del	NP_001316560.1:n.306-4411_306-4394del
XM_017017241.2:c.306-4411_306-4394del	XP_016872730.1:n.306-4411_306-4394del
XM_017017242.2:c.306-4411_306-4394del	XP_016872731.1:n.306-4411_306-4394del
XM_024448356.1:c.306-4411_306-4394del	XP_024304124.1:n.306-4411_306-4394del
XM_024448357.1:c.306-4411_306-4394del	XP_024304125.1:n.306-4411_306-4394del
XM_024448358.1:c.306-4411_306-4394del	XP_024304126.1:n.306-4411_306-4394del
XM_024448359.1:c.306-4411_306-4394del	XP_024304127.1:n.306-4411_306-4394del
XM_024448360.1:c.306-4411_306-4394del	XP_024304128.1:n.306-4411_306-4394del
XM_024448361.1:c.168-4411_168-4394del	XP_024304129.1:n.168-4411_168-4394del
XM_024448362.1:c.132-4411_132-4394del	XP_024304130.1:n.132-4411_132-4394del
XM_024448363.1:c.306-4411_306-4394del	XP_024304131.1:n.306-4411_306-4394del
XM_024448364.1:c.306-4411_306-4394del	XP_024304132.1:n.306-4411_306-4394del
XM_024448366.1:c.-13-4411_-13-4394del	XP_024304134.1:n.-13-4411_-13-4394del
XM_024448367.1:c.-13-4411_-13-4394del	XP_024304135.1:n.-13-4411_-13-4394del
XM_024448368.1:c.-13-4411_-13-4394del	XP_024304136.1:n.-13-4411_-13-4394del
XM_024448369.1:c.-14+2919_-14+2936del	XP_024304137.1:n.-14+2919_-14+2936del
XM_024448370.1:c.306-4411_306-4394del	XP_024304138.1:n.306-4411_306-4394del
XR_002957126.1:n.328-4411_328-4394del
NM_001329630.2:c.306-4411_306-4394del MANE Select	NP_001316559.1:n.306-4411_306-4394del
NM_001329631.2:c.306-4411_306-4394del	NP_001316560.1:n.306-4411_306-4394del
NM_175058.5:c.306-4411_306-4394del	NP_778228.3:n.306-4411_306-4394del