Canonical Allele Identifier: CA1151524364

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470573_6470588delinsAGCCGCTGCCGCTCCT , CM000663.2:g.6470573_6470588delinsAGCCGCTGCCGCTCCT	GRCh38
NC_000001.10:g.6530633_6530648delinsAGCCGCTGCCGCTCCT , CM000663.1:g.6530633_6530648delinsAGCCGCTGCCGCTCCT	GRCh37
NC_000001.9:g.6453220_6453235delinsAGCCGCTGCCGCTCCT	NCBI36
NG_007978.1:g.54422_54437delinsAGGAGCGGCAGCGGCT , LRG_262:g.54422_54437delinsAGGAGCGGCAGCGGCT
NG_029910.1:g.608_623delinsAGGAGCGGCAGCGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000344570.5:p.Gln533=
ENST00000377728.8:c.1598_1613delinsAGGAGCGGCAGCGGCT MANE Select	ENSP00000366957.3:p.Gln533=
ENST00000377740.5:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000366969.4:p.Gln533=
ENST00000377748.6:c.1772_1787delinsAGGAGCGGCAGCGGCT	ENSP00000366977.2:p.Gln591=
ENST00000400913.6:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000383704.1:p.Gln533=
ENST00000400915.8:c.1709_1724delinsAGGAGCGGCAGCGGCT	ENSP00000383706.4:p.Gln570=
ENST00000489097.6:n.2074_2089delinsAGGAGCGGCAGCGGCT
ENST00000535355.6:c.1805_1820delinsAGGAGCGGCAGCGGCT	ENSP00000441445.1:p.Gln602=
ENST00000537245.6:c.1709_1724delinsAGGAGCGGCAGCGGCT	ENSP00000439625.2:p.Gln570=
ENST00000673471.2:c.1895_1910delinsAGGAGCGGCAGCGGCT	ENSP00000500749.1:p.Gln632=
ENST00000674790.1:c.*1810_*1825delinsAGGAGCGGCAGCGGCT	ENSP00000502815.1:n.*1810_*1825delinsAGGAGCGGCAGCGGCT
ENST00000674943.1:n.260_275delinsAGGAGCGGCAGCGGCT
ENST00000675123.1:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000502132.1:p.Gln533=
ENST00000675548.1:c.*1426_*1441delinsAGGAGCGGCAGCGGCT	ENSP00000502684.1:n.*1426_*1441delinsAGGAGCGGCAGCGGCT
ENST00000675694.1:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000501925.1:p.Gln533=
ENST00000676401.1:n.145_160delinsAGGAGCGGCAGCGGCT
ENST00000340850.9:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000344570.5:p.Gln533=
ENST00000377725.5:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000366954.1:p.Gln533=
ENST00000377728.7:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000366957.3:p.Gln533=
ENST00000377732.5:c.1709_1724delinsAGGAGCGGCAGCGGCT	ENSP00000366961.1:p.Gln570=
ENST00000377740.4:c.1829_1844delinsAGGAGCGGCAGCGGCT	ENSP00000366969.3:p.Gln610=
ENST00000377748.5:c.1829_1844delinsAGGAGCGGCAGCGGCT	ENSP00000366977.1:p.Gln610=
ENST00000400913.5:c.1598_1613delinsAGGAGCGGCAGCGGCT	ENSP00000383704.1:p.Gln533=
ENST00000400915.7:c.1766_1781delinsAGGAGCGGCAGCGGCT	ENSP00000383706.3:p.Gln589=
ENST00000487949.4:n.800_815delinsAGGAGCGGCAGCGGCT
ENST00000489097.5:n.2074_2089delinsAGGAGCGGCAGCGGCT
ENST00000535355.5:c.1805_1820delinsAGGAGCGGCAGCGGCT	ENSP00000441445.1:p.Gln602=
ENST00000537245.5:c.1835_1850delinsAGGAGCGGCAGCGGCT	ENSP00000439625.1:p.Gln612=
NM_001042663.1:c.1766_1781delinsAGGAGCGGCAGCGGCT	NP_001036128.1:p.Gln589=
NM_001042664.1:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_001036129.1:p.Gln533=
NM_001042665.1:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_001036130.1:p.Gln533=
NM_001265592.1:c.1835_1850delinsAGGAGCGGCAGCGGCT	NP_001252521.1:p.Gln612=
NM_001265593.1:c.1805_1820delinsAGGAGCGGCAGCGGCT	NP_001252522.1:p.Gln602=
NM_001265594.1:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_001252523.1:p.Gln533=
NM_020631.4:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_065682.2:p.Gln533=
NM_198681.3:c.1829_1844delinsAGGAGCGGCAGCGGCT	NP_941374.2:p.Gln610=
NM_001042663.2:c.1766_1781delinsAGGAGCGGCAGCGGCT	NP_001036128.1:p.Gln589=
NM_001265594.2:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_001252523.1:p.Gln533=
NM_020631.5:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_065682.2:p.Gln533=
NM_001042663.3:c.1709_1724delinsAGGAGCGGCAGCGGCT	NP_001036128.2:p.Gln570=
NM_001265592.2:c.1709_1724delinsAGGAGCGGCAGCGGCT	NP_001252521.2:p.Gln570=
NM_020631.6:c.1598_1613delinsAGGAGCGGCAGCGGCT MANE Select	NP_065682.2:p.Gln533=
NM_198681.4:c.1598_1613delinsAGGAGCGGCAGCGGCT	NP_941374.3:p.Gln533=