Canonical Allele Identifier: CA338114085

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6527990T>A (hg19) ; chr1:g.6467930T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6467930T>A , CM000663.2:g.6467930T>A	GRCh38
NC_000001.10:g.6527990T>A , CM000663.1:g.6527990T>A	GRCh37
NC_000001.9:g.6450577T>A	NCBI36
NG_007978.1:g.57080A>T , LRG_262:g.57080A>T
NG_029910.1:g.3266A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2906A>T	ENSP00000344570.5:p.Gln969Leu
ENST00000377728.8:c.2906A>T MANE Select	ENSP00000366957.3:p.Gln969Leu
ENST00000377740.5:c.2906A>T	ENSP00000366969.4:p.Gln969Leu
ENST00000377748.6:c.3080A>T	ENSP00000366977.2:p.Gln1027Leu
ENST00000400913.6:c.2906A>T	ENSP00000383704.1:p.Gln969Leu
ENST00000400915.8:c.3017A>T	ENSP00000383706.4:p.Gln1006Leu
ENST00000489097.6:n.3382A>T
ENST00000535355.6:c.3113A>T	ENSP00000441445.1:p.Gln1038Leu
ENST00000537245.6:c.3017A>T	ENSP00000439625.2:p.Gln1006Leu
ENST00000673471.2:c.3203A>T	ENSP00000500749.1:p.Gln1068Leu
ENST00000674790.1:c.*3118A>T	ENSP00000502815.1:n.*3118A>T
ENST00000675123.1:c.2250-37A>T	ENSP00000502132.1:n.2250-37A>T
ENST00000675548.1:c.*2734A>T	ENSP00000502684.1:n.*2734A>T
ENST00000675694.1:c.2906A>T	ENSP00000501925.1:p.Gln969Leu
ENST00000675976.1:c.779A>T	ENSP00000501611.1:p.Gln260Leu
ENST00000340850.9:c.2906A>T	ENSP00000344570.5:p.Gln969Leu
ENST00000377725.5:c.2738-32A>T	ENSP00000366954.1:n.2738-32A>T
ENST00000377728.7:c.2906A>T	ENSP00000366957.3:p.Gln969Leu
ENST00000377732.5:c.3017A>T	ENSP00000366961.1:p.Gln1006Leu
ENST00000377740.4:c.2481-37A>T	ENSP00000366969.3:n.2481-37A>T
ENST00000377748.5:c.3137A>T	ENSP00000366977.1:p.Gln1046Leu
ENST00000400913.5:c.2906A>T	ENSP00000383704.1:p.Gln969Leu
ENST00000400915.7:c.3074A>T	ENSP00000383706.3:p.Gln1025Leu
ENST00000487949.4:n.2108A>T
ENST00000489097.5:n.3382A>T
ENST00000535355.5:c.3113A>T	ENSP00000441445.1:p.Gln1038Leu
ENST00000537245.5:c.3143A>T	ENSP00000439625.1:p.Gln1048Leu
NM_001042663.1:c.3074A>T	NP_001036128.1:p.Gln1025Leu
NM_001042664.1:c.2906A>T	NP_001036129.1:p.Gln969Leu
NM_001042665.1:c.2906A>T	NP_001036130.1:p.Gln969Leu
NM_001265592.1:c.3143A>T	NP_001252521.1:p.Gln1048Leu
NM_001265593.1:c.3113A>T	NP_001252522.1:p.Gln1038Leu
NM_001265594.1:c.2738-32A>T	NP_001252523.1:n.2738-32A>T
NM_020631.4:c.2906A>T	NP_065682.2:p.Gln969Leu
NM_198681.3:c.3137A>T	NP_941374.2:p.Gln1046Leu
NM_001042663.2:c.3074A>T	NP_001036128.1:p.Gln1025Leu
NM_001265594.2:c.2738-32A>T	NP_001252523.1:n.2738-32A>T
NM_020631.5:c.2906A>T	NP_065682.2:p.Gln969Leu
NM_001042663.3:c.3017A>T	NP_001036128.2:p.Gln1006Leu
NM_001265592.2:c.3017A>T	NP_001252521.2:p.Gln1006Leu
NM_020631.6:c.2906A>T MANE Select	NP_065682.2:p.Gln969Leu
NM_198681.4:c.2906A>T	NP_941374.3:p.Gln969Leu