Canonical Allele Identifier: CA338141883

Gene: PLEKHG5

Linked Data

• dbSNP Id: rs750665205
• gnomAD v2: 1-6537604-C-A
• gnomAD v4: 1-6477544-C-A
• MyVariant Identifiers: chr1:g.6537604C>A (hg19) ; chr1:g.6477544C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477544C>A , CM000663.2:g.6477544C>A	GRCh38
NC_000001.10:g.6537604C>A , CM000663.1:g.6537604C>A	GRCh37
NC_000001.9:g.6460191C>A	NCBI36
NG_007978.1:g.47466G>T , LRG_262:g.47466G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.28G>T	ENSP00000344570.5:p.Asp10Tyr
ENST00000377728.8:c.28G>T MANE Select	ENSP00000366957.3:p.Asp10Tyr
ENST00000377740.5:c.28G>T	ENSP00000366969.4:p.Asp10Tyr
ENST00000377748.6:c.139G>T	ENSP00000366977.2:p.Asp47Tyr
ENST00000400913.6:c.28G>T	ENSP00000383704.1:p.Asp10Tyr
ENST00000400915.8:c.139G>T	ENSP00000383706.4:p.Asp47Tyr
ENST00000489097.6:n.45G>T
ENST00000535355.6:c.235G>T	ENSP00000441445.1:p.Asp79Tyr
ENST00000537245.6:c.139G>T	ENSP00000439625.2:p.Asp47Tyr
ENST00000673471.2:c.325G>T	ENSP00000500749.1:p.Asp109Tyr
ENST00000674790.1:c.*240G>T	ENSP00000502815.1:n.*240G>T
ENST00000674803.1:n.258G>T
ENST00000675093.1:c.28G>T	ENSP00000502687.1:p.Asp10Tyr
ENST00000675123.1:c.28G>T	ENSP00000502132.1:p.Asp10Tyr
ENST00000675548.1:c.213G>T	ENSP00000502684.1:p.Ser71=
ENST00000675655.1:n.234G>T
ENST00000675694.1:c.28G>T	ENSP00000501925.1:p.Asp10Tyr
ENST00000676287.1:c.28G>T	ENSP00000502810.1:p.Asp10Tyr
ENST00000676362.1:n.251G>T
ENST00000340850.9:c.28G>T	ENSP00000344570.5:p.Asp10Tyr
ENST00000377725.5:c.28G>T	ENSP00000366954.1:p.Asp10Tyr
ENST00000377728.7:c.28G>T	ENSP00000366957.3:p.Asp10Tyr
ENST00000377732.5:c.139G>T	ENSP00000366961.1:p.Asp47Tyr
ENST00000377740.4:c.259G>T	ENSP00000366969.3:p.Asp87Tyr
ENST00000377748.5:c.259G>T	ENSP00000366977.1:p.Asp87Tyr
ENST00000400913.5:c.28G>T	ENSP00000383704.1:p.Asp10Tyr
ENST00000400915.7:c.196G>T	ENSP00000383706.3:p.Asp66Tyr
ENST00000489097.5:n.45G>T
ENST00000535355.5:c.235G>T	ENSP00000441445.1:p.Asp79Tyr
ENST00000537245.5:c.265G>T	ENSP00000439625.1:p.Asp89Tyr
NM_001042663.1:c.196G>T	NP_001036128.1:p.Asp66Tyr
NM_001042664.1:c.28G>T	NP_001036129.1:p.Asp10Tyr
NM_001042665.1:c.28G>T	NP_001036130.1:p.Asp10Tyr
NM_001265592.1:c.265G>T	NP_001252521.1:p.Asp89Tyr
NM_001265593.1:c.235G>T	NP_001252522.1:p.Asp79Tyr
NM_001265594.1:c.28G>T	NP_001252523.1:p.Asp10Tyr
NM_020631.4:c.28G>T	NP_065682.2:p.Asp10Tyr
NM_198681.3:c.259G>T	NP_941374.2:p.Asp87Tyr
NM_001042663.2:c.196G>T	NP_001036128.1:p.Asp66Tyr
NM_001265594.2:c.28G>T	NP_001252523.1:p.Asp10Tyr
NM_020631.5:c.28G>T	NP_065682.2:p.Asp10Tyr
NM_001042663.3:c.139G>T	NP_001036128.2:p.Asp47Tyr
NM_001265592.2:c.139G>T	NP_001252521.2:p.Asp47Tyr
NM_020631.6:c.28G>T MANE Select	NP_065682.2:p.Asp10Tyr
NM_198681.4:c.28G>T	NP_941374.3:p.Asp10Tyr