Canonical Allele Identifier: CA415832719

Gene: PLEKHG5

Linked Data

• ClinVar Variation Id: 2950653
• ClinVar RCV Id: RCV003809963
• dbSNP Id: rs1235218497
• gnomAD v2: 1-6532665-C-T
• gnomAD v4: 1-6472605-C-T
• MyVariant Identifiers: chr1:g.6532665C>T (hg19) ; chr1:g.6472605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6472605C>T , CM000663.2:g.6472605C>T	GRCh38
NC_000001.10:g.6532665C>T , CM000663.1:g.6532665C>T	GRCh37
NC_000001.9:g.6455252C>T	NCBI36
NG_007978.1:g.52405G>A , LRG_262:g.52405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1002G>A	ENSP00000344570.5:p.Gln334=
ENST00000377728.8:c.1002G>A MANE Select	ENSP00000366957.3:p.Gln334=
ENST00000377740.5:c.1002G>A	ENSP00000366969.4:p.Gln334=
ENST00000377748.6:c.1176G>A	ENSP00000366977.2:p.Gln392=
ENST00000400913.6:c.1002G>A	ENSP00000383704.1:p.Gln334=
ENST00000400915.8:c.1113G>A	ENSP00000383706.4:p.Gln371=
ENST00000489097.6:n.1478G>A
ENST00000535355.6:c.1209G>A	ENSP00000441445.1:p.Gln403=
ENST00000537245.6:c.1113G>A	ENSP00000439625.2:p.Gln371=
ENST00000673471.2:c.1299G>A	ENSP00000500749.1:p.Gln433=
ENST00000674790.1:c.*1214G>A	ENSP00000502815.1:n.*1214G>A
ENST00000675123.1:c.1002G>A	ENSP00000502132.1:p.Gln334=
ENST00000675548.1:c.*830G>A	ENSP00000502684.1:n.*830G>A
ENST00000675694.1:c.1002G>A	ENSP00000501925.1:p.Gln334=
ENST00000340850.9:c.1002G>A	ENSP00000344570.5:p.Gln334=
ENST00000377725.5:c.1002G>A	ENSP00000366954.1:p.Gln334=
ENST00000377728.7:c.1002G>A	ENSP00000366957.3:p.Gln334=
ENST00000377732.5:c.1113G>A	ENSP00000366961.1:p.Gln371=
ENST00000377740.4:c.1233G>A	ENSP00000366969.3:p.Gln411=
ENST00000377748.5:c.1233G>A	ENSP00000366977.1:p.Gln411=
ENST00000400913.5:c.1002G>A	ENSP00000383704.1:p.Gln334=
ENST00000400915.7:c.1170G>A	ENSP00000383706.3:p.Gln390=
ENST00000489097.5:n.1478G>A
ENST00000535355.5:c.1209G>A	ENSP00000441445.1:p.Gln403=
ENST00000537245.5:c.1239G>A	ENSP00000439625.1:p.Gln413=
NM_001042663.1:c.1170G>A	NP_001036128.1:p.Gln390=
NM_001042664.1:c.1002G>A	NP_001036129.1:p.Gln334=
NM_001042665.1:c.1002G>A	NP_001036130.1:p.Gln334=
NM_001265592.1:c.1239G>A	NP_001252521.1:p.Gln413=
NM_001265593.1:c.1209G>A	NP_001252522.1:p.Gln403=
NM_001265594.1:c.1002G>A	NP_001252523.1:p.Gln334=
NM_020631.4:c.1002G>A	NP_065682.2:p.Gln334=
NM_198681.3:c.1233G>A	NP_941374.2:p.Gln411=
NM_001042663.2:c.1170G>A	NP_001036128.1:p.Gln390=
NM_001265594.2:c.1002G>A	NP_001252523.1:p.Gln334=
NM_020631.5:c.1002G>A	NP_065682.2:p.Gln334=
NM_001042663.3:c.1113G>A	NP_001036128.2:p.Gln371=
NM_001265592.2:c.1113G>A	NP_001252521.2:p.Gln371=
NM_020631.6:c.1002G>A MANE Select	NP_065682.2:p.Gln334=
NM_198681.4:c.1002G>A	NP_941374.3:p.Gln334=