Canonical Allele Identifier: CA338142636

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6477659-C-T
• MyVariant Identifiers: chr1:g.6537719C>T (hg19) ; chr1:g.6477659C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477659C>T , CM000663.2:g.6477659C>T	GRCh38
NC_000001.10:g.6537719C>T , CM000663.1:g.6537719C>T	GRCh37
NC_000001.9:g.6460306C>T	NCBI36
NG_007978.1:g.47351G>A , LRG_262:g.47351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-87-1G>A	ENSP00000344570.5:n.-87-1G>A
ENST00000377728.8:c.-87-1G>A MANE Select	ENSP00000366957.3:n.-87-1G>A
ENST00000377740.5:c.-87-1G>A	ENSP00000366969.4:n.-87-1G>A
ENST00000377748.6:c.25-1G>A	ENSP00000366977.2:n.25-1G>A
ENST00000400913.6:c.-87-1G>A	ENSP00000383704.1:n.-87-1G>A
ENST00000400915.8:c.25-1G>A	ENSP00000383706.4:n.25-1G>A
ENST00000535355.6:c.121-1G>A	ENSP00000441445.1:n.121-1G>A
ENST00000537245.6:c.25-1G>A	ENSP00000439625.2:n.25-1G>A
ENST00000673471.2:c.211-1G>A	ENSP00000500749.1:n.211-1G>A
ENST00000674790.1:c.*126-1G>A	ENSP00000502815.1:n.*126-1G>A
ENST00000674803.1:n.144-1G>A
ENST00000675093.1:c.-87-1G>A	ENSP00000502687.1:n.-87-1G>A
ENST00000675548.1:c.99-1G>A	ENSP00000502684.1:n.99-1G>A
ENST00000675655.1:n.120-1G>A
ENST00000675694.1:c.-87-1G>A	ENSP00000501925.1:n.-87-1G>A
ENST00000676287.1:c.-87-1G>A	ENSP00000502810.1:n.-87-1G>A
ENST00000676362.1:n.137-1G>A
ENST00000340850.9:c.-87-1G>A	ENSP00000344570.5:n.-87-1G>A
ENST00000377725.5:c.-87-1G>A	ENSP00000366954.1:n.-87-1G>A
ENST00000377728.7:c.-87-1G>A	ENSP00000366957.3:n.-87-1G>A
ENST00000377732.5:c.25-1G>A	ENSP00000366961.1:n.25-1G>A
ENST00000377740.4:c.145-1G>A	ENSP00000366969.3:n.145-1G>A
ENST00000377748.5:c.145-1G>A	ENSP00000366977.1:n.145-1G>A
ENST00000400913.5:c.-87-1G>A	ENSP00000383704.1:n.-87-1G>A
ENST00000400915.7:c.82-1G>A	ENSP00000383706.3:n.82-1G>A
ENST00000535355.5:c.121-1G>A	ENSP00000441445.1:n.121-1G>A
ENST00000537245.5:c.151-1G>A	ENSP00000439625.1:n.151-1G>A
NM_001042663.1:c.82-1G>A	NP_001036128.1:n.82-1G>A
NM_001042664.1:c.-87-1G>A	NP_001036129.1:n.-87-1G>A
NM_001042665.1:c.-87-1G>A	NP_001036130.1:n.-87-1G>A
NM_001265592.1:c.151-1G>A	NP_001252521.1:n.151-1G>A
NM_001265593.1:c.121-1G>A	NP_001252522.1:n.121-1G>A
NM_001265594.1:c.-87-1G>A	NP_001252523.1:n.-87-1G>A
NM_020631.4:c.-87-1G>A	NP_065682.2:n.-87-1G>A
NM_198681.3:c.145-1G>A	NP_941374.2:n.145-1G>A
NM_001042663.2:c.82-1G>A	NP_001036128.1:n.82-1G>A
NM_001265594.2:c.-87-1G>A	NP_001252523.1:n.-87-1G>A
NM_020631.5:c.-87-1G>A	NP_065682.2:n.-87-1G>A
NM_001042663.3:c.25-1G>A	NP_001036128.2:n.25-1G>A
NM_001265592.2:c.25-1G>A	NP_001252521.2:n.25-1G>A
NM_020631.6:c.-87-1G>A MANE Select	NP_065682.2:n.-87-1G>A
NM_198681.4:c.-87-1G>A	NP_941374.3:n.-87-1G>A