Canonical Allele Identifier: CA1151524426
Gene: PLEKHG5 HGNC NCBI

Linked Data

dbSNP Id: rs993350766

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470586_6470594dup , CM000663.2:g.6470586_6470594dup GRCh38
NC_000001.10:g.6530646_6530654dup , CM000663.1:g.6530646_6530654dup GRCh37
NC_000001.9:g.6453233_6453241dup NCBI36
NG_007978.1:g.54424_54432dup , LRG_262:g.54424_54432dup
NG_029910.1:g.610_618dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1600_1608dup ENSP00000344570.5:p.Gln536_Arg537insGluArgGln
ENST00000377728.8:c.1600_1608dup MANE Select ENSP00000366957.3:p.Gln536_Arg537insGluArgGln
ENST00000377740.5:c.1600_1608dup ENSP00000366969.4:p.Gln536_Arg537insGluArgGln
ENST00000377748.6:c.1774_1782dup ENSP00000366977.2:p.Gln594_Arg595insGluArgGln
ENST00000400913.6:c.1600_1608dup ENSP00000383704.1:p.Gln536_Arg537insGluArgGln
ENST00000400915.8:c.1711_1719dup ENSP00000383706.4:p.Gln573_Arg574insGluArgGln
ENST00000489097.6:n.2076_2084dup
ENST00000535355.6:c.1807_1815dup ENSP00000441445.1:p.Gln605_Arg606insGluArgGln
ENST00000537245.6:c.1711_1719dup ENSP00000439625.2:p.Gln573_Arg574insGluArgGln
ENST00000673471.2:c.1897_1905dup ENSP00000500749.1:p.Gln635_Arg636insGluArgGln
ENST00000674790.1:c.*1812_*1820dup ENSP00000502815.1:n.*1812_*1820dup
ENST00000674943.1:n.262_270dup
ENST00000675123.1:c.1600_1608dup ENSP00000502132.1:p.Gln536_Arg537insGluArgGln
ENST00000675548.1:c.*1428_*1436dup ENSP00000502684.1:n.*1428_*1436dup
ENST00000675694.1:c.1600_1608dup ENSP00000501925.1:p.Gln536_Arg537insGluArgGln
ENST00000676401.1:n.147_155dup
ENST00000340850.9:c.1600_1608dup ENSP00000344570.5:p.Gln536_Arg537insGluArgGln
ENST00000377725.5:c.1600_1608dup ENSP00000366954.1:p.Gln536_Arg537insGluArgGln
ENST00000377728.7:c.1600_1608dup ENSP00000366957.3:p.Gln536_Arg537insGluArgGln
ENST00000377732.5:c.1711_1719dup ENSP00000366961.1:p.Gln573_Arg574insGluArgGln
ENST00000377740.4:c.1831_1839dup ENSP00000366969.3:p.Gln613_Arg614insGluArgGln
ENST00000377748.5:c.1831_1839dup ENSP00000366977.1:p.Gln613_Arg614insGluArgGln
ENST00000400913.5:c.1600_1608dup ENSP00000383704.1:p.Gln536_Arg537insGluArgGln
ENST00000400915.7:c.1768_1776dup ENSP00000383706.3:p.Gln592_Arg593insGluArgGln
ENST00000487949.4:n.802_810dup
ENST00000489097.5:n.2076_2084dup
ENST00000535355.5:c.1807_1815dup ENSP00000441445.1:p.Gln605_Arg606insGluArgGln
ENST00000537245.5:c.1837_1845dup ENSP00000439625.1:p.Gln615_Arg616insGluArgGln
NM_001042663.1:c.1768_1776dup NP_001036128.1:p.Gln592_Arg593insGluArgGln
NM_001042664.1:c.1600_1608dup NP_001036129.1:p.Gln536_Arg537insGluArgGln
NM_001042665.1:c.1600_1608dup NP_001036130.1:p.Gln536_Arg537insGluArgGln
NM_001265592.1:c.1837_1845dup NP_001252521.1:p.Gln615_Arg616insGluArgGln
NM_001265593.1:c.1807_1815dup NP_001252522.1:p.Gln605_Arg606insGluArgGln
NM_001265594.1:c.1600_1608dup NP_001252523.1:p.Gln536_Arg537insGluArgGln
NM_020631.4:c.1600_1608dup NP_065682.2:p.Gln536_Arg537insGluArgGln
NM_198681.3:c.1831_1839dup NP_941374.2:p.Gln613_Arg614insGluArgGln
NM_001042663.2:c.1768_1776dup NP_001036128.1:p.Gln592_Arg593insGluArgGln
NM_001265594.2:c.1600_1608dup NP_001252523.1:p.Gln536_Arg537insGluArgGln
NM_020631.5:c.1600_1608dup NP_065682.2:p.Gln536_Arg537insGluArgGln
NM_001042663.3:c.1711_1719dup NP_001036128.2:p.Gln573_Arg574insGluArgGln
NM_001265592.2:c.1711_1719dup NP_001252521.2:p.Gln573_Arg574insGluArgGln
NM_020631.6:c.1600_1608dup MANE Select NP_065682.2:p.Gln536_Arg537insGluArgGln
NM_198681.4:c.1600_1608dup NP_941374.3:p.Gln536_Arg537insGluArgGln