Canonical Allele Identifier: CA218407684
Gene: PLEKHA7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.16802189G>T , CM000673.2:g.16802189G>T GRCh38
NC_000011.9:g.16823736G>T , CM000673.1:g.16823736G>T GRCh37
NC_000011.8:g.16780312G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696749.1:c.2029-372C>A ENSP00000512848.1:n.2029-372C>A
ENST00000698836.1:c.2158-372C>A ENSP00000513972.1:n.2158-372C>A
ENST00000531066.6:c.2158-372C>A MANE Select ENSP00000435389.1:n.2158-372C>A
ENST00000636113.1:c.373-372C>A ENSP00000490177.1:n.373-372C>A
ENST00000637162.1:c.1973-372C>A
ENST00000355661.7:c.2158-372C>A ENSP00000347883.2:n.2158-372C>A
ENST00000525049.5:n.354-372C>A
ENST00000525581.2:c.151-372C>A ENSP00000431455.1:n.151-372C>A
ENST00000525781.5:n.908-372C>A
ENST00000530489.5:c.1050-372C>A
ENST00000531066.5:c.2158-372C>A ENSP00000435389.1:n.2158-372C>A
ENST00000531079.1:n.389-372C>A
ENST00000532079.1:c.82-12320C>A ENSP00000434812.1:n.82-12320C>A
NM_175058.4:c.2158-372C>A NP_778228.3:n.2158-372C>A
XM_006718149.2:c.2359-372C>A XP_006718212.1:n.2359-372C>A
XM_011519910.1:c.2221-372C>A XP_011518212.1:n.2221-372C>A
XM_011519911.1:c.2185-372C>A XP_011518213.1:n.2185-372C>A
XM_011519912.1:c.2155-372C>A XP_011518214.1:n.2155-372C>A
XM_011519913.1:c.2104-372C>A XP_011518215.1:n.2104-372C>A
XM_011519914.1:c.2158-372C>A XP_011518216.1:n.2158-372C>A
XM_011519915.1:c.2077-372C>A XP_011518217.1:n.2077-372C>A
XM_011519916.1:c.2104-372C>A XP_011518218.1:n.2104-372C>A
XM_011519917.1:c.1648-372C>A XP_011518219.1:n.1648-372C>A
XM_011519918.1:c.880-372C>A XP_011518220.1:n.880-372C>A
NM_001329630.1:c.2158-372C>A NP_001316559.1:n.2158-372C>A
NM_001329631.1:c.2158-372C>A NP_001316560.1:n.2158-372C>A
XM_017017241.2:c.2359-372C>A XP_016872730.1:n.2359-372C>A
XM_017017242.2:c.2239-372C>A XP_016872731.1:n.2239-372C>A
XM_024448356.1:c.2359-372C>A XP_024304124.1:n.2359-372C>A
XM_024448357.1:c.2359-372C>A XP_024304125.1:n.2359-372C>A
XM_024448358.1:c.2359-372C>A XP_024304126.1:n.2359-372C>A
XM_024448359.1:c.2278-372C>A XP_024304127.1:n.2278-372C>A
XM_024448360.1:c.2239-372C>A XP_024304128.1:n.2239-372C>A
XM_024448361.1:c.2221-372C>A XP_024304129.1:n.2221-372C>A
XM_024448362.1:c.2185-372C>A XP_024304130.1:n.2185-372C>A
XM_024448363.1:c.2158-372C>A XP_024304131.1:n.2158-372C>A
XM_024448364.1:c.2158-372C>A XP_024304132.1:n.2158-372C>A
XM_024448365.1:c.2077-372C>A XP_024304133.1:n.2077-372C>A
XM_024448366.1:c.2041-372C>A XP_024304134.1:n.2041-372C>A
XM_024448367.1:c.2041-372C>A XP_024304135.1:n.2041-372C>A
XM_024448368.1:c.2041-372C>A XP_024304136.1:n.2041-372C>A
XM_024448369.1:c.2041-372C>A XP_024304137.1:n.2041-372C>A
XM_024448370.1:c.2359-372C>A XP_024304138.1:n.2359-372C>A
XR_002957126.1:n.2381-372C>A
NM_001329630.2:c.2158-372C>A MANE Select NP_001316559.1:n.2158-372C>A
NM_001329631.2:c.2158-372C>A NP_001316560.1:n.2158-372C>A
NM_175058.5:c.2158-372C>A NP_778228.3:n.2158-372C>A
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