Canonical Allele Identifier: CA1143497856

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469466C= , CM000663.2:g.6469466C=	GRCh38
NC_000001.10:g.6529526C= , CM000663.1:g.6529526C=	GRCh37
NC_000001.9:g.6452113C=	NCBI36
NG_007978.1:g.55544G= , LRG_262:g.55544G=
NG_029910.1:g.1730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1934-16G=	ENSP00000344570.5:n.1934-16G=
ENST00000377728.8:c.1934-16G= MANE Select	ENSP00000366957.3:n.1934-16G=
ENST00000377740.5:c.1934-16G=	ENSP00000366969.4:n.1934-16G=
ENST00000377748.6:c.2108-16G=	ENSP00000366977.2:n.2108-16G=
ENST00000400913.6:c.1934-16G=	ENSP00000383704.1:n.1934-16G=
ENST00000400915.8:c.2045-16G=	ENSP00000383706.4:n.2045-16G=
ENST00000489097.6:n.2410-16G=
ENST00000535355.6:c.2141-16G=	ENSP00000441445.1:n.2141-16G=
ENST00000537245.6:c.2045-16G=	ENSP00000439625.2:n.2045-16G=
ENST00000673471.2:c.2231-16G=	ENSP00000500749.1:n.2231-16G=
ENST00000674790.1:c.*2146-16G=	ENSP00000502815.1:n.*2146-16G=
ENST00000675123.1:c.1934-16G=	ENSP00000502132.1:n.1934-16G=
ENST00000675548.1:c.*1762-16G=	ENSP00000502684.1:n.*1762-16G=
ENST00000675694.1:c.1934-16G=	ENSP00000501925.1:n.1934-16G=
ENST00000676401.1:n.481-16G=
ENST00000340850.9:c.1934-16G=	ENSP00000344570.5:n.1934-16G=
ENST00000377725.5:c.1934-16G=	ENSP00000366954.1:n.1934-16G=
ENST00000377728.7:c.1934-16G=	ENSP00000366957.3:n.1934-16G=
ENST00000377732.5:c.2045-16G=	ENSP00000366961.1:n.2045-16G=
ENST00000377740.4:c.2165-16G=	ENSP00000366969.3:n.2165-16G=
ENST00000377748.5:c.2165-16G=	ENSP00000366977.1:n.2165-16G=
ENST00000400913.5:c.1934-16G=	ENSP00000383704.1:n.1934-16G=
ENST00000400915.7:c.2102-16G=	ENSP00000383706.3:n.2102-16G=
ENST00000487949.4:n.1136-16G=
ENST00000489097.5:n.2410-16G=
ENST00000535355.5:c.2141-16G=	ENSP00000441445.1:n.2141-16G=
ENST00000537245.5:c.2171-16G=	ENSP00000439625.1:n.2171-16G=
NM_001042663.1:c.2102-16G=	NP_001036128.1:n.2102-16G=
NM_001042664.1:c.1934-16G=	NP_001036129.1:n.1934-16G=
NM_001042665.1:c.1934-16G=	NP_001036130.1:n.1934-16G=
NM_001265592.1:c.2171-16G=	NP_001252521.1:n.2171-16G=
NM_001265593.1:c.2141-16G=	NP_001252522.1:n.2141-16G=
NM_001265594.1:c.1934-16G=	NP_001252523.1:n.1934-16G=
NM_020631.4:c.1934-16G=	NP_065682.2:n.1934-16G=
NM_198681.3:c.2165-16G=	NP_941374.2:n.2165-16G=
NM_001042663.2:c.2102-16G=	NP_001036128.1:n.2102-16G=
NM_001265594.2:c.1934-16G=	NP_001252523.1:n.1934-16G=
NM_020631.5:c.1934-16G=	NP_065682.2:n.1934-16G=
NM_001042663.3:c.2045-16G=	NP_001036128.2:n.2045-16G=
NM_001265592.2:c.2045-16G=	NP_001252521.2:n.2045-16G=
NM_020631.6:c.1934-16G= MANE Select	NP_065682.2:n.1934-16G=
NM_198681.4:c.1934-16G=	NP_941374.3:n.1934-16G=