Canonical Allele Identifier: CA416022672

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6468193-G-A
• MyVariant Identifiers: chr1:g.6528253G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468193G>A , CM000663.2:g.6468193G>A	GRCh38
NC_000001.10:g.6528253G>A , CM000663.1:g.6528253G>A	GRCh37
NC_000001.9:g.6450840G>A	NCBI36
NG_007978.1:g.56817C>T , LRG_262:g.56817C>T
NG_029910.1:g.3003C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2643C>T	ENSP00000344570.5:p.Ser881=
ENST00000377728.8:c.2643C>T MANE Select	ENSP00000366957.3:p.Ser881=
ENST00000377740.5:c.2643C>T	ENSP00000366969.4:p.Ser881=
ENST00000377748.6:c.2817C>T	ENSP00000366977.2:p.Ser939=
ENST00000400913.6:c.2643C>T	ENSP00000383704.1:p.Ser881=
ENST00000400915.8:c.2754C>T	ENSP00000383706.4:p.Ser918=
ENST00000489097.6:n.3119C>T
ENST00000535355.6:c.2850C>T	ENSP00000441445.1:p.Ser950=
ENST00000537245.6:c.2754C>T	ENSP00000439625.2:p.Ser918=
ENST00000673471.2:c.2940C>T	ENSP00000500749.1:p.Ser980=
ENST00000674790.1:c.*2855C>T	ENSP00000502815.1:n.*2855C>T
ENST00000675123.1:c.2250-300C>T	ENSP00000502132.1:n.2250-300C>T
ENST00000675548.1:c.*2471C>T	ENSP00000502684.1:n.*2471C>T
ENST00000675694.1:c.2643C>T	ENSP00000501925.1:p.Ser881=
ENST00000675976.1:c.516C>T	ENSP00000501611.1:p.Ser172=
ENST00000340850.9:c.2643C>T	ENSP00000344570.5:p.Ser881=
ENST00000377725.5:c.2643C>T	ENSP00000366954.1:p.Ser881=
ENST00000377728.7:c.2643C>T	ENSP00000366957.3:p.Ser881=
ENST00000377732.5:c.2754C>T	ENSP00000366961.1:p.Ser918=
ENST00000377740.4:c.2481-300C>T	ENSP00000366969.3:n.2481-300C>T
ENST00000377748.5:c.2874C>T	ENSP00000366977.1:p.Ser958=
ENST00000400913.5:c.2643C>T	ENSP00000383704.1:p.Ser881=
ENST00000400915.7:c.2811C>T	ENSP00000383706.3:p.Ser937=
ENST00000487949.4:n.1845C>T
ENST00000489097.5:n.3119C>T
ENST00000535355.5:c.2850C>T	ENSP00000441445.1:p.Ser950=
ENST00000537245.5:c.2880C>T	ENSP00000439625.1:p.Ser960=
NM_001042663.1:c.2811C>T	NP_001036128.1:p.Ser937=
NM_001042664.1:c.2643C>T	NP_001036129.1:p.Ser881=
NM_001042665.1:c.2643C>T	NP_001036130.1:p.Ser881=
NM_001265592.1:c.2880C>T	NP_001252521.1:p.Ser960=
NM_001265593.1:c.2850C>T	NP_001252522.1:p.Ser950=
NM_001265594.1:c.2643C>T	NP_001252523.1:p.Ser881=
NM_020631.4:c.2643C>T	NP_065682.2:p.Ser881=
NM_198681.3:c.2874C>T	NP_941374.2:p.Ser958=
NM_001042663.2:c.2811C>T	NP_001036128.1:p.Ser937=
NM_001265594.2:c.2643C>T	NP_001252523.1:p.Ser881=
NM_020631.5:c.2643C>T	NP_065682.2:p.Ser881=
NM_001042663.3:c.2754C>T	NP_001036128.2:p.Ser918=
NM_001265592.2:c.2754C>T	NP_001252521.2:p.Ser918=
NM_020631.6:c.2643C>T MANE Select	NP_065682.2:p.Ser881=
NM_198681.4:c.2643C>T	NP_941374.3:p.Ser881=