Canonical Allele Identifier: CA2642977897

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6474294-A-ACCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474297_6474298insCCCCCCC , CM000663.2:g.6474297_6474298insCCCCCCC	GRCh38
NC_000001.10:g.6534357_6534358insCCCCCCC , CM000663.1:g.6534357_6534358insCCCCCCC	GRCh37
NC_000001.9:g.6456944_6456945insCCCCCCC	NCBI36
NG_007978.1:g.50715_50716insGGGGGGG , LRG_262:g.50715_50716insGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.440-131_440-130insGGGGGGG	ENSP00000344570.5:n.440-131_440-130insGGGGGGG
ENST00000377728.8:c.440-131_440-130insGGGGGGG MANE Select	ENSP00000366957.3:n.440-131_440-130insGGGGGGG
ENST00000377740.5:c.440-131_440-130insGGGGGGG	ENSP00000366969.4:n.440-131_440-130insGGGGGGG
ENST00000377748.6:c.614-131_614-130insGGGGGGG	ENSP00000366977.2:n.614-131_614-130insGGGGGGG
ENST00000400913.6:c.440-131_440-130insGGGGGGG	ENSP00000383704.1:n.440-131_440-130insGGGGGGG
ENST00000400915.8:c.551-131_551-130insGGGGGGG	ENSP00000383706.4:n.551-131_551-130insGGGGGGG
ENST00000489097.6:n.916-131_916-130insGGGGGGG
ENST00000535355.6:c.647-131_647-130insGGGGGGG	ENSP00000441445.1:n.647-131_647-130insGGGGGGG
ENST00000537245.6:c.551-131_551-130insGGGGGGG	ENSP00000439625.2:n.551-131_551-130insGGGGGGG
ENST00000673471.2:c.737-131_737-130insGGGGGGG	ENSP00000500749.1:n.737-131_737-130insGGGGGGG
ENST00000674790.1:c.*652-131_*652-130insGGGGGGG	ENSP00000502815.1:n.*652-131_*652-130insGGGGGGG
ENST00000675123.1:c.440-131_440-130insGGGGGGG	ENSP00000502132.1:n.440-131_440-130insGGGGGGG
ENST00000675548.1:c.*268-131_*268-130insGGGGGGG	ENSP00000502684.1:n.*268-131_*268-130insGGGGGGG
ENST00000675694.1:c.440-131_440-130insGGGGGGG	ENSP00000501925.1:n.440-131_440-130insGGGGGGG
ENST00000340850.9:c.440-131_440-130insGGGGGGG	ENSP00000344570.5:n.440-131_440-130insGGGGGGG
ENST00000377725.5:c.440-131_440-130insGGGGGGG	ENSP00000366954.1:n.440-131_440-130insGGGGGGG
ENST00000377728.7:c.440-131_440-130insGGGGGGG	ENSP00000366957.3:n.440-131_440-130insGGGGGGG
ENST00000377732.5:c.551-131_551-130insGGGGGGG	ENSP00000366961.1:n.551-131_551-130insGGGGGGG
ENST00000377740.4:c.671-131_671-130insGGGGGGG	ENSP00000366969.3:n.671-131_671-130insGGGGGGG
ENST00000377748.5:c.671-131_671-130insGGGGGGG	ENSP00000366977.1:n.671-131_671-130insGGGGGGG
ENST00000400913.5:c.440-131_440-130insGGGGGGG	ENSP00000383704.1:n.440-131_440-130insGGGGGGG
ENST00000400915.7:c.608-131_608-130insGGGGGGG	ENSP00000383706.3:n.608-131_608-130insGGGGGGG
ENST00000489097.5:n.916-131_916-130insGGGGGGG
ENST00000535355.5:c.647-131_647-130insGGGGGGG	ENSP00000441445.1:n.647-131_647-130insGGGGGGG
ENST00000537245.5:c.677-131_677-130insGGGGGGG	ENSP00000439625.1:n.677-131_677-130insGGGGGGG
NM_001042663.1:c.608-131_608-130insGGGGGGG	NP_001036128.1:n.608-131_608-130insGGGGGGG
NM_001042664.1:c.440-131_440-130insGGGGGGG	NP_001036129.1:n.440-131_440-130insGGGGGGG
NM_001042665.1:c.440-131_440-130insGGGGGGG	NP_001036130.1:n.440-131_440-130insGGGGGGG
NM_001265592.1:c.677-131_677-130insGGGGGGG	NP_001252521.1:n.677-131_677-130insGGGGGGG
NM_001265593.1:c.647-131_647-130insGGGGGGG	NP_001252522.1:n.647-131_647-130insGGGGGGG
NM_001265594.1:c.440-131_440-130insGGGGGGG	NP_001252523.1:n.440-131_440-130insGGGGGGG
NM_020631.4:c.440-131_440-130insGGGGGGG	NP_065682.2:n.440-131_440-130insGGGGGGG
NM_198681.3:c.671-131_671-130insGGGGGGG	NP_941374.2:n.671-131_671-130insGGGGGGG
NM_001042663.2:c.608-131_608-130insGGGGGGG	NP_001036128.1:n.608-131_608-130insGGGGGGG
NM_001265594.2:c.440-131_440-130insGGGGGGG	NP_001252523.1:n.440-131_440-130insGGGGGGG
NM_020631.5:c.440-131_440-130insGGGGGGG	NP_065682.2:n.440-131_440-130insGGGGGGG
NM_001042663.3:c.551-131_551-130insGGGGGGG	NP_001036128.2:n.551-131_551-130insGGGGGGG
NM_001265592.2:c.551-131_551-130insGGGGGGG	NP_001252521.2:n.551-131_551-130insGGGGGGG
NM_020631.6:c.440-131_440-130insGGGGGGG MANE Select	NP_065682.2:n.440-131_440-130insGGGGGGG
NM_198681.4:c.440-131_440-130insGGGGGGG	NP_941374.3:n.440-131_440-130insGGGGGGG