Canonical Allele Identifier: CA1151507588

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474776C= , CM000663.2:g.6474776C=	GRCh38
NC_000001.10:g.6534836C= , CM000663.1:g.6534836C=	GRCh37
NC_000001.9:g.6457423C=	NCBI36
NG_007978.1:g.50234G= , LRG_262:g.50234G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.303-189G=	ENSP00000344570.5:n.303-189G=
ENST00000377728.8:c.303-189G= MANE Select	ENSP00000366957.3:n.303-189G=
ENST00000377740.5:c.303-189G=	ENSP00000366969.4:n.303-189G=
ENST00000377748.6:c.477-189G=	ENSP00000366977.2:n.477-189G=
ENST00000400913.6:c.303-189G=	ENSP00000383704.1:n.303-189G=
ENST00000400915.8:c.414-189G=	ENSP00000383706.4:n.414-189G=
ENST00000489097.6:n.590G=
ENST00000535355.6:c.510-189G=	ENSP00000441445.1:n.510-189G=
ENST00000537245.6:c.414-189G=	ENSP00000439625.2:n.414-189G=
ENST00000673471.2:c.600-189G=	ENSP00000500749.1:n.600-189G=
ENST00000674790.1:c.*515-189G=	ENSP00000502815.1:n.*515-189G=
ENST00000675093.1:c.303-189G=	ENSP00000502687.1:n.303-189G=
ENST00000675123.1:c.303-189G=	ENSP00000502132.1:n.303-189G=
ENST00000675548.1:c.*131-189G=	ENSP00000502684.1:n.*131-189G=
ENST00000675694.1:c.303-189G=	ENSP00000501925.1:n.303-189G=
ENST00000676255.1:c.185G=	ENSP00000502459.1:n.185G=
ENST00000676287.1:c.303-189G=	ENSP00000502810.1:n.303-189G=
ENST00000340850.9:c.303-189G=	ENSP00000344570.5:n.303-189G=
ENST00000377725.5:c.303-189G=	ENSP00000366954.1:n.303-189G=
ENST00000377728.7:c.303-189G=	ENSP00000366957.3:n.303-189G=
ENST00000377732.5:c.414-189G=	ENSP00000366961.1:n.414-189G=
ENST00000377740.4:c.534-189G=	ENSP00000366969.3:n.534-189G=
ENST00000377748.5:c.534-189G=	ENSP00000366977.1:n.534-189G=
ENST00000400913.5:c.303-189G=	ENSP00000383704.1:n.303-189G=
ENST00000400915.7:c.471-189G=	ENSP00000383706.3:n.471-189G=
ENST00000489097.5:n.590G=
ENST00000535355.5:c.510-189G=	ENSP00000441445.1:n.510-189G=
ENST00000537245.5:c.540-189G=	ENSP00000439625.1:n.540-189G=
NM_001042663.1:c.471-189G=	NP_001036128.1:n.471-189G=
NM_001042664.1:c.303-189G=	NP_001036129.1:n.303-189G=
NM_001042665.1:c.303-189G=	NP_001036130.1:n.303-189G=
NM_001265592.1:c.540-189G=	NP_001252521.1:n.540-189G=
NM_001265593.1:c.510-189G=	NP_001252522.1:n.510-189G=
NM_001265594.1:c.303-189G=	NP_001252523.1:n.303-189G=
NM_020631.4:c.303-189G=	NP_065682.2:n.303-189G=
NM_198681.3:c.534-189G=	NP_941374.2:n.534-189G=
NM_001042663.2:c.471-189G=	NP_001036128.1:n.471-189G=
NM_001265594.2:c.303-189G=	NP_001252523.1:n.303-189G=
NM_020631.5:c.303-189G=	NP_065682.2:n.303-189G=
NM_001042663.3:c.414-189G=	NP_001036128.2:n.414-189G=
NM_001265592.2:c.414-189G=	NP_001252521.2:n.414-189G=
NM_020631.6:c.303-189G= MANE Select	NP_065682.2:n.303-189G=
NM_198681.4:c.303-189G=	NP_941374.3:n.303-189G=