Canonical Allele Identifier: CA338139496

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6534610C>A (hg19) ; chr1:g.6474550C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474550C>A , CM000663.2:g.6474550C>A	GRCh38
NC_000001.10:g.6534610C>A , CM000663.1:g.6534610C>A	GRCh37
NC_000001.9:g.6457197C>A	NCBI36
NG_007978.1:g.50460G>T , LRG_262:g.50460G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.340G>T	ENSP00000344570.5:p.Ala114Ser
ENST00000377728.8:c.340G>T MANE Select	ENSP00000366957.3:p.Ala114Ser
ENST00000377740.5:c.340G>T	ENSP00000366969.4:p.Ala114Ser
ENST00000377748.6:c.514G>T	ENSP00000366977.2:p.Ala172Ser
ENST00000400913.6:c.340G>T	ENSP00000383704.1:p.Ala114Ser
ENST00000400915.8:c.451G>T	ENSP00000383706.4:p.Ala151Ser
ENST00000489097.6:n.816G>T
ENST00000535355.6:c.547G>T	ENSP00000441445.1:p.Ala183Ser
ENST00000537245.6:c.451G>T	ENSP00000439625.2:p.Ala151Ser
ENST00000673471.2:c.637G>T	ENSP00000500749.1:p.Ala213Ser
ENST00000674790.1:c.*552G>T	ENSP00000502815.1:n.*552G>T
ENST00000675123.1:c.340G>T	ENSP00000502132.1:p.Ala114Ser
ENST00000675548.1:c.*168G>T	ENSP00000502684.1:n.*168G>T
ENST00000675694.1:c.340G>T	ENSP00000501925.1:p.Ala114Ser
ENST00000676255.1:c.302G>T	ENSP00000502459.1:n.302G>T
ENST00000340850.9:c.340G>T	ENSP00000344570.5:p.Ala114Ser
ENST00000377725.5:c.340G>T	ENSP00000366954.1:p.Ala114Ser
ENST00000377728.7:c.340G>T	ENSP00000366957.3:p.Ala114Ser
ENST00000377732.5:c.451G>T	ENSP00000366961.1:p.Ala151Ser
ENST00000377740.4:c.571G>T	ENSP00000366969.3:p.Ala191Ser
ENST00000377748.5:c.571G>T	ENSP00000366977.1:p.Ala191Ser
ENST00000400913.5:c.340G>T	ENSP00000383704.1:p.Ala114Ser
ENST00000400915.7:c.508G>T	ENSP00000383706.3:p.Ala170Ser
ENST00000489097.5:n.816G>T
ENST00000535355.5:c.547G>T	ENSP00000441445.1:p.Ala183Ser
ENST00000537245.5:c.577G>T	ENSP00000439625.1:p.Ala193Ser
NM_001042663.1:c.508G>T	NP_001036128.1:p.Ala170Ser
NM_001042664.1:c.340G>T	NP_001036129.1:p.Ala114Ser
NM_001042665.1:c.340G>T	NP_001036130.1:p.Ala114Ser
NM_001265592.1:c.577G>T	NP_001252521.1:p.Ala193Ser
NM_001265593.1:c.547G>T	NP_001252522.1:p.Ala183Ser
NM_001265594.1:c.340G>T	NP_001252523.1:p.Ala114Ser
NM_020631.4:c.340G>T	NP_065682.2:p.Ala114Ser
NM_198681.3:c.571G>T	NP_941374.2:p.Ala191Ser
NM_001042663.2:c.508G>T	NP_001036128.1:p.Ala170Ser
NM_001265594.2:c.340G>T	NP_001252523.1:p.Ala114Ser
NM_020631.5:c.340G>T	NP_065682.2:p.Ala114Ser
NM_001042663.3:c.451G>T	NP_001036128.2:p.Ala151Ser
NM_001265592.2:c.451G>T	NP_001252521.2:p.Ala151Ser
NM_020631.6:c.340G>T MANE Select	NP_065682.2:p.Ala114Ser
NM_198681.4:c.340G>T	NP_941374.3:p.Ala114Ser