Canonical Allele Identifier: CA1151525598

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470823_6470825delinsTGG , CM000663.2:g.6470823_6470825delinsTGG	GRCh38
NC_000001.10:g.6530883_6530885delinsTGG , CM000663.1:g.6530883_6530885delinsTGG	GRCh37
NC_000001.9:g.6453470_6453472delinsTGG	NCBI36
NG_007978.1:g.54185_54187delinsCCA , LRG_262:g.54185_54187delinsCCA
NG_029910.1:g.371_373delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1452_1454delinsCCA	ENSP00000344570.5:p.Pro484=
ENST00000377728.8:c.1452_1454delinsCCA MANE Select	ENSP00000366957.3:p.Pro484=
ENST00000377740.5:c.1452_1454delinsCCA	ENSP00000366969.4:p.Pro484=
ENST00000377748.6:c.1626_1628delinsCCA	ENSP00000366977.2:p.Pro542=
ENST00000400913.6:c.1452_1454delinsCCA	ENSP00000383704.1:p.Pro484=
ENST00000400915.8:c.1563_1565delinsCCA	ENSP00000383706.4:p.Pro521=
ENST00000489097.6:n.1928_1930delinsCCA
ENST00000535355.6:c.1659_1661delinsCCA	ENSP00000441445.1:p.Pro553=
ENST00000537245.6:c.1563_1565delinsCCA	ENSP00000439625.2:p.Pro521=
ENST00000673471.2:c.1749_1751delinsCCA	ENSP00000500749.1:p.Pro583=
ENST00000674685.1:n.485_487delinsCCA
ENST00000674790.1:c.*1664_*1666delinsCCA	ENSP00000502815.1:n.*1664_*1666delinsCCA
ENST00000674943.1:n.114_116delinsCCA
ENST00000675123.1:c.1452_1454delinsCCA	ENSP00000502132.1:p.Pro484=
ENST00000675548.1:c.*1280_*1282delinsCCA	ENSP00000502684.1:n.*1280_*1282delinsCCA
ENST00000675694.1:c.1452_1454delinsCCA	ENSP00000501925.1:p.Pro484=
ENST00000340850.9:c.1452_1454delinsCCA	ENSP00000344570.5:p.Pro484=
ENST00000377725.5:c.1452_1454delinsCCA	ENSP00000366954.1:p.Pro484=
ENST00000377728.7:c.1452_1454delinsCCA	ENSP00000366957.3:p.Pro484=
ENST00000377732.5:c.1563_1565delinsCCA	ENSP00000366961.1:p.Pro521=
ENST00000377740.4:c.1683_1685delinsCCA	ENSP00000366969.3:p.Pro561=
ENST00000377748.5:c.1683_1685delinsCCA	ENSP00000366977.1:p.Pro561=
ENST00000400913.5:c.1452_1454delinsCCA	ENSP00000383704.1:p.Pro484=
ENST00000400915.7:c.1620_1622delinsCCA	ENSP00000383706.3:p.Pro540=
ENST00000487949.4:n.654_656delinsCCA
ENST00000489097.5:n.1928_1930delinsCCA
ENST00000535355.5:c.1659_1661delinsCCA	ENSP00000441445.1:p.Pro553=
ENST00000537245.5:c.1689_1691delinsCCA	ENSP00000439625.1:p.Pro563=
NM_001042663.1:c.1620_1622delinsCCA	NP_001036128.1:p.Pro540=
NM_001042664.1:c.1452_1454delinsCCA	NP_001036129.1:p.Pro484=
NM_001042665.1:c.1452_1454delinsCCA	NP_001036130.1:p.Pro484=
NM_001265592.1:c.1689_1691delinsCCA	NP_001252521.1:p.Pro563=
NM_001265593.1:c.1659_1661delinsCCA	NP_001252522.1:p.Pro553=
NM_001265594.1:c.1452_1454delinsCCA	NP_001252523.1:p.Pro484=
NM_020631.4:c.1452_1454delinsCCA	NP_065682.2:p.Pro484=
NM_198681.3:c.1683_1685delinsCCA	NP_941374.2:p.Pro561=
NM_001042663.2:c.1620_1622delinsCCA	NP_001036128.1:p.Pro540=
NM_001265594.2:c.1452_1454delinsCCA	NP_001252523.1:p.Pro484=
NM_020631.5:c.1452_1454delinsCCA	NP_065682.2:p.Pro484=
NM_001042663.3:c.1563_1565delinsCCA	NP_001036128.2:p.Pro521=
NM_001265592.2:c.1563_1565delinsCCA	NP_001252521.2:p.Pro521=
NM_020631.6:c.1452_1454delinsCCA MANE Select	NP_065682.2:p.Pro484=
NM_198681.4:c.1452_1454delinsCCA	NP_941374.3:p.Pro484=