Canonical Allele Identifier: CA338141850

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6537597G>C (hg19) ; chr1:g.6477537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477537G>C , CM000663.2:g.6477537G>C	GRCh38
NC_000001.10:g.6537597G>C , CM000663.1:g.6537597G>C	GRCh37
NC_000001.9:g.6460184G>C	NCBI36
NG_007978.1:g.47473C>G , LRG_262:g.47473C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.35C>G	ENSP00000344570.5:p.Pro12Arg
ENST00000377728.8:c.35C>G MANE Select	ENSP00000366957.3:p.Pro12Arg
ENST00000377740.5:c.35C>G	ENSP00000366969.4:p.Pro12Arg
ENST00000377748.6:c.146C>G	ENSP00000366977.2:p.Pro49Arg
ENST00000400913.6:c.35C>G	ENSP00000383704.1:p.Pro12Arg
ENST00000400915.8:c.146C>G	ENSP00000383706.4:p.Pro49Arg
ENST00000489097.6:n.52C>G
ENST00000535355.6:c.242C>G	ENSP00000441445.1:p.Pro81Arg
ENST00000537245.6:c.146C>G	ENSP00000439625.2:p.Pro49Arg
ENST00000673471.2:c.332C>G	ENSP00000500749.1:p.Pro111Arg
ENST00000674790.1:c.*247C>G	ENSP00000502815.1:n.*247C>G
ENST00000674803.1:n.265C>G
ENST00000675093.1:c.35C>G	ENSP00000502687.1:p.Pro12Arg
ENST00000675123.1:c.35C>G	ENSP00000502132.1:p.Pro12Arg
ENST00000675548.1:c.220C>G	ENSP00000502684.1:p.Pro74Ala
ENST00000675655.1:n.241C>G
ENST00000675694.1:c.35C>G	ENSP00000501925.1:p.Pro12Arg
ENST00000676287.1:c.35C>G	ENSP00000502810.1:p.Pro12Arg
ENST00000676362.1:n.258C>G
ENST00000340850.9:c.35C>G	ENSP00000344570.5:p.Pro12Arg
ENST00000377725.5:c.35C>G	ENSP00000366954.1:p.Pro12Arg
ENST00000377728.7:c.35C>G	ENSP00000366957.3:p.Pro12Arg
ENST00000377732.5:c.146C>G	ENSP00000366961.1:p.Pro49Arg
ENST00000377740.4:c.266C>G	ENSP00000366969.3:p.Pro89Arg
ENST00000377748.5:c.266C>G	ENSP00000366977.1:p.Pro89Arg
ENST00000400913.5:c.35C>G	ENSP00000383704.1:p.Pro12Arg
ENST00000400915.7:c.203C>G	ENSP00000383706.3:p.Pro68Arg
ENST00000489097.5:n.52C>G
ENST00000535355.5:c.242C>G	ENSP00000441445.1:p.Pro81Arg
ENST00000537245.5:c.272C>G	ENSP00000439625.1:p.Pro91Arg
NM_001042663.1:c.203C>G	NP_001036128.1:p.Pro68Arg
NM_001042664.1:c.35C>G	NP_001036129.1:p.Pro12Arg
NM_001042665.1:c.35C>G	NP_001036130.1:p.Pro12Arg
NM_001265592.1:c.272C>G	NP_001252521.1:p.Pro91Arg
NM_001265593.1:c.242C>G	NP_001252522.1:p.Pro81Arg
NM_001265594.1:c.35C>G	NP_001252523.1:p.Pro12Arg
NM_020631.4:c.35C>G	NP_065682.2:p.Pro12Arg
NM_198681.3:c.266C>G	NP_941374.2:p.Pro89Arg
NM_001042663.2:c.203C>G	NP_001036128.1:p.Pro68Arg
NM_001265594.2:c.35C>G	NP_001252523.1:p.Pro12Arg
NM_020631.5:c.35C>G	NP_065682.2:p.Pro12Arg
NM_001042663.3:c.146C>G	NP_001036128.2:p.Pro49Arg
NM_001265592.2:c.146C>G	NP_001252521.2:p.Pro49Arg
NM_020631.6:c.35C>G MANE Select	NP_065682.2:p.Pro12Arg
NM_198681.4:c.35C>G	NP_941374.3:p.Pro12Arg