Canonical Allele Identifier: CA1143627610

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6467904C= , CM000663.2:g.6467904C=	GRCh38
NC_000001.10:g.6527964C= , CM000663.1:g.6527964C=	GRCh37
NC_000001.9:g.6450551C=	NCBI36
NG_007978.1:g.57106G= , LRG_262:g.57106G=
NG_029910.1:g.3292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2932G=	ENSP00000344570.5:p.Ala978=
ENST00000377728.8:c.2932G= MANE Select	ENSP00000366957.3:p.Ala978=
ENST00000377740.5:c.2932G=	ENSP00000366969.4:p.Ala978=
ENST00000377748.6:c.3106G=	ENSP00000366977.2:p.Ala1036=
ENST00000400913.6:c.2932G=	ENSP00000383704.1:p.Ala978=
ENST00000400915.8:c.3043G=	ENSP00000383706.4:p.Ala1015=
ENST00000489097.6:n.3408G=
ENST00000535355.6:c.3139G=	ENSP00000441445.1:p.Ala1047=
ENST00000537245.6:c.3043G=	ENSP00000439625.2:p.Ala1015=
ENST00000673471.2:c.3229G=	ENSP00000500749.1:p.Ala1077=
ENST00000674790.1:c.*3144G=	ENSP00000502815.1:n.*3144G=
ENST00000675123.1:c.2250-11G=	ENSP00000502132.1:n.2250-11G=
ENST00000675548.1:c.*2760G=	ENSP00000502684.1:n.*2760G=
ENST00000675694.1:c.2932G=	ENSP00000501925.1:p.Ala978=
ENST00000675976.1:c.805G=	ENSP00000501611.1:p.Ala269=
ENST00000340850.9:c.2932G=	ENSP00000344570.5:p.Ala978=
ENST00000377725.5:c.2738-6G=	ENSP00000366954.1:n.2738-6G=
ENST00000377728.7:c.2932G=	ENSP00000366957.3:p.Ala978=
ENST00000377732.5:c.3043G=	ENSP00000366961.1:p.Ala1015=
ENST00000377740.4:c.2481-11G=	ENSP00000366969.3:n.2481-11G=
ENST00000377748.5:c.3163G=	ENSP00000366977.1:p.Ala1055=
ENST00000400913.5:c.2932G=	ENSP00000383704.1:p.Ala978=
ENST00000400915.7:c.3100G=	ENSP00000383706.3:p.Ala1034=
ENST00000487949.4:n.2134G=
ENST00000489097.5:n.3408G=
ENST00000535355.5:c.3139G=	ENSP00000441445.1:p.Ala1047=
ENST00000537245.5:c.3169G=	ENSP00000439625.1:p.Ala1057=
NM_001042663.1:c.3100G=	NP_001036128.1:p.Ala1034=
NM_001042664.1:c.2932G=	NP_001036129.1:p.Ala978=
NM_001042665.1:c.2932G=	NP_001036130.1:p.Ala978=
NM_001265592.1:c.3169G=	NP_001252521.1:p.Ala1057=
NM_001265593.1:c.3139G=	NP_001252522.1:p.Ala1047=
NM_001265594.1:c.2738-6G=	NP_001252523.1:n.2738-6G=
NM_020631.4:c.2932G=	NP_065682.2:p.Ala978=
NM_198681.3:c.3163G=	NP_941374.2:p.Ala1055=
NM_001042663.2:c.3100G=	NP_001036128.1:p.Ala1034=
NM_001265594.2:c.2738-6G=	NP_001252523.1:n.2738-6G=
NM_020631.5:c.2932G=	NP_065682.2:p.Ala978=
NM_001042663.3:c.3043G=	NP_001036128.2:p.Ala1015=
NM_001265592.2:c.3043G=	NP_001252521.2:p.Ala1015=
NM_020631.6:c.2932G= MANE Select	NP_065682.2:p.Ala978=
NM_198681.4:c.2932G=	NP_941374.3:p.Ala978=