Canonical Allele Identifier: CA416022441

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6468082-G-A
• MyVariant Identifiers: chr1:g.6528142G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468082G>A , CM000663.2:g.6468082G>A	GRCh38
NC_000001.10:g.6528142G>A , CM000663.1:g.6528142G>A	GRCh37
NC_000001.9:g.6450729G>A	NCBI36
NG_007978.1:g.56928C>T , LRG_262:g.56928C>T
NG_029910.1:g.3114C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.2754C>T	ENSP00000344570.5:p.Gly918=
ENST00000377728.8:c.2754C>T MANE Select	ENSP00000366957.3:p.Gly918=
ENST00000377740.5:c.2754C>T	ENSP00000366969.4:p.Gly918=
ENST00000377748.6:c.2928C>T	ENSP00000366977.2:p.Gly976=
ENST00000400913.6:c.2754C>T	ENSP00000383704.1:p.Gly918=
ENST00000400915.8:c.2865C>T	ENSP00000383706.4:p.Gly955=
ENST00000489097.6:n.3230C>T
ENST00000535355.6:c.2961C>T	ENSP00000441445.1:p.Gly987=
ENST00000537245.6:c.2865C>T	ENSP00000439625.2:p.Gly955=
ENST00000673471.2:c.3051C>T	ENSP00000500749.1:p.Gly1017=
ENST00000674790.1:c.*2966C>T	ENSP00000502815.1:n.*2966C>T
ENST00000675123.1:c.2250-189C>T	ENSP00000502132.1:n.2250-189C>T
ENST00000675548.1:c.*2582C>T	ENSP00000502684.1:n.*2582C>T
ENST00000675694.1:c.2754C>T	ENSP00000501925.1:p.Gly918=
ENST00000675976.1:c.627C>T	ENSP00000501611.1:p.Gly209=
ENST00000340850.9:c.2754C>T	ENSP00000344570.5:p.Gly918=
ENST00000377725.5:c.2737+17C>T	ENSP00000366954.1:n.2737+17C>T
ENST00000377728.7:c.2754C>T	ENSP00000366957.3:p.Gly918=
ENST00000377732.5:c.2865C>T	ENSP00000366961.1:p.Gly955=
ENST00000377740.4:c.2481-189C>T	ENSP00000366969.3:n.2481-189C>T
ENST00000377748.5:c.2985C>T	ENSP00000366977.1:p.Gly995=
ENST00000400913.5:c.2754C>T	ENSP00000383704.1:p.Gly918=
ENST00000400915.7:c.2922C>T	ENSP00000383706.3:p.Gly974=
ENST00000487949.4:n.1956C>T
ENST00000489097.5:n.3230C>T
ENST00000535355.5:c.2961C>T	ENSP00000441445.1:p.Gly987=
ENST00000537245.5:c.2991C>T	ENSP00000439625.1:p.Gly997=
NM_001042663.1:c.2922C>T	NP_001036128.1:p.Gly974=
NM_001042664.1:c.2754C>T	NP_001036129.1:p.Gly918=
NM_001042665.1:c.2754C>T	NP_001036130.1:p.Gly918=
NM_001265592.1:c.2991C>T	NP_001252521.1:p.Gly997=
NM_001265593.1:c.2961C>T	NP_001252522.1:p.Gly987=
NM_001265594.1:c.2737+17C>T	NP_001252523.1:n.2737+17C>T
NM_020631.4:c.2754C>T	NP_065682.2:p.Gly918=
NM_198681.3:c.2985C>T	NP_941374.2:p.Gly995=
NM_001042663.2:c.2922C>T	NP_001036128.1:p.Gly974=
NM_001265594.2:c.2737+17C>T	NP_001252523.1:n.2737+17C>T
NM_020631.5:c.2754C>T	NP_065682.2:p.Gly918=
NM_001042663.3:c.2865C>T	NP_001036128.2:p.Gly955=
NM_001265592.2:c.2865C>T	NP_001252521.2:p.Gly955=
NM_020631.6:c.2754C>T MANE Select	NP_065682.2:p.Gly918=
NM_198681.4:c.2754C>T	NP_941374.3:p.Gly918=