Canonical Allele Identifier: CA1151507048

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474574G= , CM000663.2:g.6474574G=	GRCh38
NC_000001.10:g.6534634G= , CM000663.1:g.6534634G=	GRCh37
NC_000001.9:g.6457221G=	NCBI36
NG_007978.1:g.50436C= , LRG_262:g.50436C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.316C=	ENSP00000344570.5:p.Pro106=
ENST00000377728.8:c.316C= MANE Select	ENSP00000366957.3:p.Pro106=
ENST00000377740.5:c.316C=	ENSP00000366969.4:p.Pro106=
ENST00000377748.6:c.490C=	ENSP00000366977.2:p.Pro164=
ENST00000400913.6:c.316C=	ENSP00000383704.1:p.Pro106=
ENST00000400915.8:c.427C=	ENSP00000383706.4:p.Pro143=
ENST00000489097.6:n.792C=
ENST00000535355.6:c.523C=	ENSP00000441445.1:p.Pro175=
ENST00000537245.6:c.427C=	ENSP00000439625.2:p.Pro143=
ENST00000673471.2:c.613C=	ENSP00000500749.1:p.Pro205=
ENST00000674790.1:c.*528C=	ENSP00000502815.1:n.*528C=
ENST00000675123.1:c.316C=	ENSP00000502132.1:p.Pro106=
ENST00000675548.1:c.*144C=	ENSP00000502684.1:n.*144C=
ENST00000675694.1:c.316C=	ENSP00000501925.1:p.Pro106=
ENST00000676255.1:c.278C=	ENSP00000502459.1:n.278C=
ENST00000340850.9:c.316C=	ENSP00000344570.5:p.Pro106=
ENST00000377725.5:c.316C=	ENSP00000366954.1:p.Pro106=
ENST00000377728.7:c.316C=	ENSP00000366957.3:p.Pro106=
ENST00000377732.5:c.427C=	ENSP00000366961.1:p.Pro143=
ENST00000377740.4:c.547C=	ENSP00000366969.3:p.Pro183=
ENST00000377748.5:c.547C=	ENSP00000366977.1:p.Pro183=
ENST00000400913.5:c.316C=	ENSP00000383704.1:p.Pro106=
ENST00000400915.7:c.484C=	ENSP00000383706.3:p.Pro162=
ENST00000489097.5:n.792C=
ENST00000535355.5:c.523C=	ENSP00000441445.1:p.Pro175=
ENST00000537245.5:c.553C=	ENSP00000439625.1:p.Pro185=
NM_001042663.1:c.484C=	NP_001036128.1:p.Pro162=
NM_001042664.1:c.316C=	NP_001036129.1:p.Pro106=
NM_001042665.1:c.316C=	NP_001036130.1:p.Pro106=
NM_001265592.1:c.553C=	NP_001252521.1:p.Pro185=
NM_001265593.1:c.523C=	NP_001252522.1:p.Pro175=
NM_001265594.1:c.316C=	NP_001252523.1:p.Pro106=
NM_020631.4:c.316C=	NP_065682.2:p.Pro106=
NM_198681.3:c.547C=	NP_941374.2:p.Pro183=
NM_001042663.2:c.484C=	NP_001036128.1:p.Pro162=
NM_001265594.2:c.316C=	NP_001252523.1:p.Pro106=
NM_020631.5:c.316C=	NP_065682.2:p.Pro106=
NM_001042663.3:c.427C=	NP_001036128.2:p.Pro143=
NM_001265592.2:c.427C=	NP_001252521.2:p.Pro143=
NM_020631.6:c.316C= MANE Select	NP_065682.2:p.Pro106=
NM_198681.4:c.316C=	NP_941374.3:p.Pro106=