Canonical Allele Identifier: CA156017972
Gene: PLEKHA8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10488084

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30043405A>C , CM000669.2:g.30043405A>C GRCh38
NC_000007.12:g.30049546A>C NCBI36
NC_000007.13:g.30083021A>C , CM000669.1:g.30083021A>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000258679.11:c.41-1680A>C ENSP00000258679.7:p.=
ENST00000396257.6:c.41-1680A>C ENSP00000379556.2:p.=
ENST00000396259.5:c.41-1680A>C ENSP00000379558.1:p.=
ENST00000440706.2:n.119-1680A>C ENSP00000407802.1:p.=
ENST00000449726.5:c.41-1680A>C ENSP00000397947.1:p.=
ENST00000483799.5:n.145-1680A>C
ENST00000622102.4:c.41-1680A>C ENSP00000484427.1:p.=
NM_001197026.1:c.41-1680A>C VV NP_001183955.1:p.=
NM_001197027.1:c.41-1680A>C VV NP_001183956.1:p.=
NM_032639.3:c.41-1680A>C VV NP_116028.1:p.=
XM_005249897.2:c.41-1680A>C XP_005249954.1:p.=
XM_005249898.1:c.-480-1680A>C XP_005249955.1:p.=
XM_011515591.1:c.41-1680A>C XP_011513893.1:p.=
XM_011515592.1:c.41-1680A>C XP_011513894.1:p.=
XM_011515593.1:c.41-1680A>C XP_011513895.1:p.=
XM_011515594.1:c.41-1680A>C XP_011513896.1:p.=
XM_011515595.1:c.41-1680A>C XP_011513897.1:p.=
NM_001350973.1:c.41-1680A>C VV NP_001337902.1:p.=
NM_001350974.1:c.41-1680A>C VV NP_001337903.1:p.=
NM_001350975.1:c.-616-1680A>C VV NP_001337904.1:p.=
NM_001363473.1:c.41-1680A>C VV NP_001350402.1:p.=
XM_011515591.2:c.41-1680A>C
XM_011515592.3:c.41-1680A>C
XM_017012744.1:c.41-1680A>C XP_016868233.1:p.=
XM_017012746.1:c.-616-1680A>C XP_016868235.1:p.=
XM_017012747.1:c.-649-1680A>C XP_016868236.1:p.=