Canonical Allele Identifier: CA415835543

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6477587-G-A
• MyVariant Identifiers: chr1:g.6537647G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477587G>A , CM000663.2:g.6477587G>A	GRCh38
NC_000001.10:g.6537647G>A , CM000663.1:g.6537647G>A	GRCh37
NC_000001.9:g.6460234G>A	NCBI36
NG_007978.1:g.47423C>T , LRG_262:g.47423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-16C>T	ENSP00000344570.5:n.-16C>T
ENST00000377728.8:c.-16C>T MANE Select	ENSP00000366957.3:n.-16C>T
ENST00000377740.5:c.-16C>T	ENSP00000366969.4:n.-16C>T
ENST00000377748.6:c.96C>T	ENSP00000366977.2:p.Ser32=
ENST00000400913.6:c.-16C>T	ENSP00000383704.1:n.-16C>T
ENST00000400915.8:c.96C>T	ENSP00000383706.4:p.Ser32=
ENST00000489097.6:n.2C>T
ENST00000535355.6:c.192C>T	ENSP00000441445.1:p.Ser64=
ENST00000537245.6:c.96C>T	ENSP00000439625.2:p.Ser32=
ENST00000673471.2:c.282C>T	ENSP00000500749.1:p.Ser94=
ENST00000674790.1:c.*197C>T	ENSP00000502815.1:n.*197C>T
ENST00000674803.1:n.215C>T
ENST00000675093.1:c.-16C>T	ENSP00000502687.1:n.-16C>T
ENST00000675123.1:c.-16C>T	ENSP00000502132.1:n.-16C>T
ENST00000675548.1:c.170C>T	ENSP00000502684.1:p.Ala57Val
ENST00000675655.1:n.191C>T
ENST00000675694.1:c.-16C>T	ENSP00000501925.1:n.-16C>T
ENST00000676287.1:c.-16C>T	ENSP00000502810.1:n.-16C>T
ENST00000676362.1:n.208C>T
ENST00000340850.9:c.-16C>T	ENSP00000344570.5:n.-16C>T
ENST00000377725.5:c.-16C>T	ENSP00000366954.1:n.-16C>T
ENST00000377728.7:c.-16C>T	ENSP00000366957.3:n.-16C>T
ENST00000377732.5:c.96C>T	ENSP00000366961.1:p.Ser32=
ENST00000377740.4:c.216C>T	ENSP00000366969.3:p.Ser72=
ENST00000377748.5:c.216C>T	ENSP00000366977.1:p.Ser72=
ENST00000400913.5:c.-16C>T	ENSP00000383704.1:n.-16C>T
ENST00000400915.7:c.153C>T	ENSP00000383706.3:p.Ser51=
ENST00000489097.5:n.2C>T
ENST00000535355.5:c.192C>T	ENSP00000441445.1:p.Ser64=
ENST00000537245.5:c.222C>T	ENSP00000439625.1:p.Ser74=
NM_001042663.1:c.153C>T	NP_001036128.1:p.Ser51=
NM_001042664.1:c.-16C>T	NP_001036129.1:n.-16C>T
NM_001042665.1:c.-16C>T	NP_001036130.1:n.-16C>T
NM_001265592.1:c.222C>T	NP_001252521.1:p.Ser74=
NM_001265593.1:c.192C>T	NP_001252522.1:p.Ser64=
NM_001265594.1:c.-16C>T	NP_001252523.1:n.-16C>T
NM_020631.4:c.-16C>T	NP_065682.2:n.-16C>T
NM_198681.3:c.216C>T	NP_941374.2:p.Ser72=
NM_001042663.2:c.153C>T	NP_001036128.1:p.Ser51=
NM_001265594.2:c.-16C>T	NP_001252523.1:n.-16C>T
NM_020631.5:c.-16C>T	NP_065682.2:n.-16C>T
NM_001042663.3:c.96C>T	NP_001036128.2:p.Ser32=
NM_001265592.2:c.96C>T	NP_001252521.2:p.Ser32=
NM_020631.6:c.-16C>T MANE Select	NP_065682.2:n.-16C>T
NM_198681.4:c.-16C>T	NP_941374.3:n.-16C>T