Canonical Allele Identifier: CA338114058

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6527987G>A (hg19) ; chr1:g.6467927G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6467927G>A , CM000663.2:g.6467927G>A	GRCh38
NC_000001.10:g.6527987G>A , CM000663.1:g.6527987G>A	GRCh37
NC_000001.9:g.6450574G>A	NCBI36
NG_007978.1:g.57083C>T , LRG_262:g.57083C>T
NG_029910.1:g.3269C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2909C>T	ENSP00000344570.5:p.Pro970Leu
ENST00000377728.8:c.2909C>T MANE Select	ENSP00000366957.3:p.Pro970Leu
ENST00000377740.5:c.2909C>T	ENSP00000366969.4:p.Pro970Leu
ENST00000377748.6:c.3083C>T	ENSP00000366977.2:p.Pro1028Leu
ENST00000400913.6:c.2909C>T	ENSP00000383704.1:p.Pro970Leu
ENST00000400915.8:c.3020C>T	ENSP00000383706.4:p.Pro1007Leu
ENST00000489097.6:n.3385C>T
ENST00000535355.6:c.3116C>T	ENSP00000441445.1:p.Pro1039Leu
ENST00000537245.6:c.3020C>T	ENSP00000439625.2:p.Pro1007Leu
ENST00000673471.2:c.3206C>T	ENSP00000500749.1:p.Pro1069Leu
ENST00000674790.1:c.*3121C>T	ENSP00000502815.1:n.*3121C>T
ENST00000675123.1:c.2250-34C>T	ENSP00000502132.1:n.2250-34C>T
ENST00000675548.1:c.*2737C>T	ENSP00000502684.1:n.*2737C>T
ENST00000675694.1:c.2909C>T	ENSP00000501925.1:p.Pro970Leu
ENST00000675976.1:c.782C>T	ENSP00000501611.1:p.Pro261Leu
ENST00000340850.9:c.2909C>T	ENSP00000344570.5:p.Pro970Leu
ENST00000377725.5:c.2738-29C>T	ENSP00000366954.1:n.2738-29C>T
ENST00000377728.7:c.2909C>T	ENSP00000366957.3:p.Pro970Leu
ENST00000377732.5:c.3020C>T	ENSP00000366961.1:p.Pro1007Leu
ENST00000377740.4:c.2481-34C>T	ENSP00000366969.3:n.2481-34C>T
ENST00000377748.5:c.3140C>T	ENSP00000366977.1:p.Pro1047Leu
ENST00000400913.5:c.2909C>T	ENSP00000383704.1:p.Pro970Leu
ENST00000400915.7:c.3077C>T	ENSP00000383706.3:p.Pro1026Leu
ENST00000487949.4:n.2111C>T
ENST00000489097.5:n.3385C>T
ENST00000535355.5:c.3116C>T	ENSP00000441445.1:p.Pro1039Leu
ENST00000537245.5:c.3146C>T	ENSP00000439625.1:p.Pro1049Leu
NM_001042663.1:c.3077C>T	NP_001036128.1:p.Pro1026Leu
NM_001042664.1:c.2909C>T	NP_001036129.1:p.Pro970Leu
NM_001042665.1:c.2909C>T	NP_001036130.1:p.Pro970Leu
NM_001265592.1:c.3146C>T	NP_001252521.1:p.Pro1049Leu
NM_001265593.1:c.3116C>T	NP_001252522.1:p.Pro1039Leu
NM_001265594.1:c.2738-29C>T	NP_001252523.1:n.2738-29C>T
NM_020631.4:c.2909C>T	NP_065682.2:p.Pro970Leu
NM_198681.3:c.3140C>T	NP_941374.2:p.Pro1047Leu
NM_001042663.2:c.3077C>T	NP_001036128.1:p.Pro1026Leu
NM_001265594.2:c.2738-29C>T	NP_001252523.1:n.2738-29C>T
NM_020631.5:c.2909C>T	NP_065682.2:p.Pro970Leu
NM_001042663.3:c.3020C>T	NP_001036128.2:p.Pro1007Leu
NM_001265592.2:c.3020C>T	NP_001252521.2:p.Pro1007Leu
NM_020631.6:c.2909C>T MANE Select	NP_065682.2:p.Pro970Leu
NM_198681.4:c.2909C>T	NP_941374.3:p.Pro970Leu