Canonical Allele Identifier: CA17246475

Gene: PLEKHG5

Linked Data

• dbSNP Id: rs750665205
• gnomAD v3: 1-6477544-C-T
• gnomAD v4: 1-6477544-C-T
• COSMIC: COSM3491778 ; COSM4905820 ; COSM4905821
• MyVariant Identifiers: chr1:g.6537604C>T (hg19) ; chr1:g.6477544C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477544C>T , CM000663.2:g.6477544C>T	GRCh38
NC_000001.10:g.6537604C>T , CM000663.1:g.6537604C>T	GRCh37
NC_000001.9:g.6460191C>T	NCBI36
NG_007978.1:g.47466G>A , LRG_262:g.47466G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.28G>A	ENSP00000344570.5:p.Asp10Asn
ENST00000377728.8:c.28G>A MANE Select	ENSP00000366957.3:p.Asp10Asn
ENST00000377740.5:c.28G>A	ENSP00000366969.4:p.Asp10Asn
ENST00000377748.6:c.139G>A	ENSP00000366977.2:p.Asp47Asn
ENST00000400913.6:c.28G>A	ENSP00000383704.1:p.Asp10Asn
ENST00000400915.8:c.139G>A	ENSP00000383706.4:p.Asp47Asn
ENST00000489097.6:n.45G>A
ENST00000535355.6:c.235G>A	ENSP00000441445.1:p.Asp79Asn
ENST00000537245.6:c.139G>A	ENSP00000439625.2:p.Asp47Asn
ENST00000673471.2:c.325G>A	ENSP00000500749.1:p.Asp109Asn
ENST00000674790.1:c.*240G>A	ENSP00000502815.1:n.*240G>A
ENST00000674803.1:n.258G>A
ENST00000675093.1:c.28G>A	ENSP00000502687.1:p.Asp10Asn
ENST00000675123.1:c.28G>A	ENSP00000502132.1:p.Asp10Asn
ENST00000675548.1:c.213G>A	ENSP00000502684.1:p.Ser71=
ENST00000675655.1:n.234G>A
ENST00000675694.1:c.28G>A	ENSP00000501925.1:p.Asp10Asn
ENST00000676287.1:c.28G>A	ENSP00000502810.1:p.Asp10Asn
ENST00000676362.1:n.251G>A
ENST00000340850.9:c.28G>A	ENSP00000344570.5:p.Asp10Asn
ENST00000377725.5:c.28G>A	ENSP00000366954.1:p.Asp10Asn
ENST00000377728.7:c.28G>A	ENSP00000366957.3:p.Asp10Asn
ENST00000377732.5:c.139G>A	ENSP00000366961.1:p.Asp47Asn
ENST00000377740.4:c.259G>A	ENSP00000366969.3:p.Asp87Asn
ENST00000377748.5:c.259G>A	ENSP00000366977.1:p.Asp87Asn
ENST00000400913.5:c.28G>A	ENSP00000383704.1:p.Asp10Asn
ENST00000400915.7:c.196G>A	ENSP00000383706.3:p.Asp66Asn
ENST00000489097.5:n.45G>A
ENST00000535355.5:c.235G>A	ENSP00000441445.1:p.Asp79Asn
ENST00000537245.5:c.265G>A	ENSP00000439625.1:p.Asp89Asn
NM_001042663.1:c.196G>A	NP_001036128.1:p.Asp66Asn
NM_001042664.1:c.28G>A	NP_001036129.1:p.Asp10Asn
NM_001042665.1:c.28G>A	NP_001036130.1:p.Asp10Asn
NM_001265592.1:c.265G>A	NP_001252521.1:p.Asp89Asn
NM_001265593.1:c.235G>A	NP_001252522.1:p.Asp79Asn
NM_001265594.1:c.28G>A	NP_001252523.1:p.Asp10Asn
NM_020631.4:c.28G>A	NP_065682.2:p.Asp10Asn
NM_198681.3:c.259G>A	NP_941374.2:p.Asp87Asn
NM_001042663.2:c.196G>A	NP_001036128.1:p.Asp66Asn
NM_001265594.2:c.28G>A	NP_001252523.1:p.Asp10Asn
NM_020631.5:c.28G>A	NP_065682.2:p.Asp10Asn
NM_001042663.3:c.139G>A	NP_001036128.2:p.Asp47Asn
NM_001265592.2:c.139G>A	NP_001252521.2:p.Asp47Asn
NM_020631.6:c.28G>A MANE Select	NP_065682.2:p.Asp10Asn
NM_198681.4:c.28G>A	NP_941374.3:p.Asp10Asn