Canonical Allele Identifier: CA1151498640

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6471079_6471080delinsAG , CM000663.2:g.6471079_6471080delinsAG	GRCh38
NC_000001.10:g.6531139_6531140delinsAG , CM000663.1:g.6531139_6531140delinsAG	GRCh37
NC_000001.9:g.6453726_6453727delinsAG	NCBI36
NG_007978.1:g.53930_53931delinsCT , LRG_262:g.53930_53931delinsCT
NG_029910.1:g.116_117delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1302_1303delinsCT	ENSP00000344570.5:p.Pro434=
ENST00000377728.8:c.1302_1303delinsCT MANE Select	ENSP00000366957.3:p.Pro434=
ENST00000377740.5:c.1302_1303delinsCT	ENSP00000366969.4:p.Pro434=
ENST00000377748.6:c.1476_1477delinsCT	ENSP00000366977.2:p.Pro492=
ENST00000400913.6:c.1302_1303delinsCT	ENSP00000383704.1:p.Pro434=
ENST00000400915.8:c.1413_1414delinsCT	ENSP00000383706.4:p.Pro471=
ENST00000489097.6:n.1778_1779delinsCT
ENST00000535355.6:c.1509_1510delinsCT	ENSP00000441445.1:p.Pro503=
ENST00000537245.6:c.1413_1414delinsCT	ENSP00000439625.2:p.Pro471=
ENST00000673471.2:c.1599_1600delinsCT	ENSP00000500749.1:p.Pro533=
ENST00000674685.1:n.335_336delinsCT
ENST00000674790.1:c.*1514_*1515delinsCT	ENSP00000502815.1:n.*1514_*1515delinsCT
ENST00000675123.1:c.1302_1303delinsCT	ENSP00000502132.1:p.Pro434=
ENST00000675548.1:c.*1130_*1131delinsCT	ENSP00000502684.1:n.*1130_*1131delinsCT
ENST00000675694.1:c.1302_1303delinsCT	ENSP00000501925.1:p.Pro434=
ENST00000340850.9:c.1302_1303delinsCT	ENSP00000344570.5:p.Pro434=
ENST00000377725.5:c.1302_1303delinsCT	ENSP00000366954.1:p.Pro434=
ENST00000377728.7:c.1302_1303delinsCT	ENSP00000366957.3:p.Pro434=
ENST00000377732.5:c.1413_1414delinsCT	ENSP00000366961.1:p.Pro471=
ENST00000377740.4:c.1533_1534delinsCT	ENSP00000366969.3:p.Pro511=
ENST00000377748.5:c.1533_1534delinsCT	ENSP00000366977.1:p.Pro511=
ENST00000400913.5:c.1302_1303delinsCT	ENSP00000383704.1:p.Pro434=
ENST00000400915.7:c.1470_1471delinsCT	ENSP00000383706.3:p.Pro490=
ENST00000487949.4:n.504_505delinsCT
ENST00000489097.5:n.1778_1779delinsCT
ENST00000535355.5:c.1509_1510delinsCT	ENSP00000441445.1:p.Pro503=
ENST00000537245.5:c.1539_1540delinsCT	ENSP00000439625.1:p.Pro513=
NM_001042663.1:c.1470_1471delinsCT	NP_001036128.1:p.Pro490=
NM_001042664.1:c.1302_1303delinsCT	NP_001036129.1:p.Pro434=
NM_001042665.1:c.1302_1303delinsCT	NP_001036130.1:p.Pro434=
NM_001265592.1:c.1539_1540delinsCT	NP_001252521.1:p.Pro513=
NM_001265593.1:c.1509_1510delinsCT	NP_001252522.1:p.Pro503=
NM_001265594.1:c.1302_1303delinsCT	NP_001252523.1:p.Pro434=
NM_020631.4:c.1302_1303delinsCT	NP_065682.2:p.Pro434=
NM_198681.3:c.1533_1534delinsCT	NP_941374.2:p.Pro511=
NM_001042663.2:c.1470_1471delinsCT	NP_001036128.1:p.Pro490=
NM_001265594.2:c.1302_1303delinsCT	NP_001252523.1:p.Pro434=
NM_020631.5:c.1302_1303delinsCT	NP_065682.2:p.Pro434=
NM_001042663.3:c.1413_1414delinsCT	NP_001036128.2:p.Pro471=
NM_001265592.2:c.1413_1414delinsCT	NP_001252521.2:p.Pro471=
NM_020631.6:c.1302_1303delinsCT MANE Select	NP_065682.2:p.Pro434=
NM_198681.4:c.1302_1303delinsCT	NP_941374.3:p.Pro434=