Canonical Allele Identifier: CA338113749

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6527952T>A (hg19) ; chr1:g.6467892T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6467892T>A , CM000663.2:g.6467892T>A	GRCh38
NC_000001.10:g.6527952T>A , CM000663.1:g.6527952T>A	GRCh37
NC_000001.9:g.6450539T>A	NCBI36
NG_007978.1:g.57118A>T , LRG_262:g.57118A>T
NG_029910.1:g.3304A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.2944A>T	ENSP00000344570.5:p.Lys982Ter
ENST00000377728.8:c.2944A>T MANE Select	ENSP00000366957.3:p.Lys982Ter
ENST00000377740.5:c.2944A>T	ENSP00000366969.4:p.Lys982Ter
ENST00000377748.6:c.3118A>T	ENSP00000366977.2:p.Lys1040Ter
ENST00000400913.6:c.2944A>T	ENSP00000383704.1:p.Lys982Ter
ENST00000400915.8:c.3055A>T	ENSP00000383706.4:p.Lys1019Ter
ENST00000489097.6:n.3420A>T
ENST00000535355.6:c.3151A>T	ENSP00000441445.1:p.Lys1051Ter
ENST00000537245.6:c.3055A>T	ENSP00000439625.2:p.Lys1019Ter
ENST00000673471.2:c.3241A>T	ENSP00000500749.1:p.Lys1081Ter
ENST00000674790.1:c.*3156A>T	ENSP00000502815.1:n.*3156A>T
ENST00000675123.1:c.2251A>T	ENSP00000502132.1:p.Lys751Ter
ENST00000675548.1:c.*2772A>T	ENSP00000502684.1:n.*2772A>T
ENST00000675694.1:c.2944A>T	ENSP00000501925.1:p.Lys982Ter
ENST00000675976.1:c.817A>T	ENSP00000501611.1:p.Lys273Ter
ENST00000340850.9:c.2944A>T	ENSP00000344570.5:p.Lys982Ter
ENST00000377725.5:c.2744A>T	ENSP00000366954.1:p.Glu915Val
ENST00000377728.7:c.2944A>T	ENSP00000366957.3:p.Lys982Ter
ENST00000377732.5:c.3055A>T	ENSP00000366961.1:p.Lys1019Ter
ENST00000377740.4:c.2482A>T	ENSP00000366969.3:p.Lys828Ter
ENST00000377748.5:c.3175A>T	ENSP00000366977.1:p.Lys1059Ter
ENST00000400913.5:c.2944A>T	ENSP00000383704.1:p.Lys982Ter
ENST00000400915.7:c.3112A>T	ENSP00000383706.3:p.Lys1038Ter
ENST00000487949.4:n.2146A>T
ENST00000489097.5:n.3420A>T
ENST00000535355.5:c.3151A>T	ENSP00000441445.1:p.Lys1051Ter
ENST00000537245.5:c.3181A>T	ENSP00000439625.1:p.Lys1061Ter
NM_001042663.1:c.3112A>T	NP_001036128.1:p.Lys1038Ter
NM_001042664.1:c.2944A>T	NP_001036129.1:p.Lys982Ter
NM_001042665.1:c.2944A>T	NP_001036130.1:p.Lys982Ter
NM_001265592.1:c.3181A>T	NP_001252521.1:p.Lys1061Ter
NM_001265593.1:c.3151A>T	NP_001252522.1:p.Lys1051Ter
NM_001265594.1:c.2744A>T	NP_001252523.1:p.Glu915Val
NM_020631.4:c.2944A>T	NP_065682.2:p.Lys982Ter
NM_198681.3:c.3175A>T	NP_941374.2:p.Lys1059Ter
NM_001042663.2:c.3112A>T	NP_001036128.1:p.Lys1038Ter
NM_001265594.2:c.2744A>T	NP_001252523.1:p.Glu915Val
NM_020631.5:c.2944A>T	NP_065682.2:p.Lys982Ter
NM_001042663.3:c.3055A>T	NP_001036128.2:p.Lys1019Ter
NM_001265592.2:c.3055A>T	NP_001252521.2:p.Lys1019Ter
NM_020631.6:c.2944A>T MANE Select	NP_065682.2:p.Lys982Ter
NM_198681.4:c.2944A>T	NP_941374.3:p.Lys982Ter