Canonical Allele Identifier: CA415834161

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6474551-A-G
• MyVariant Identifiers: chr1:g.6534611A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474551A>G , CM000663.2:g.6474551A>G	GRCh38
NC_000001.10:g.6534611A>G , CM000663.1:g.6534611A>G	GRCh37
NC_000001.9:g.6457198A>G	NCBI36
NG_007978.1:g.50459T>C , LRG_262:g.50459T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.339T>C	ENSP00000344570.5:p.Ile113=
ENST00000377728.8:c.339T>C MANE Select	ENSP00000366957.3:p.Ile113=
ENST00000377740.5:c.339T>C	ENSP00000366969.4:p.Ile113=
ENST00000377748.6:c.513T>C	ENSP00000366977.2:p.Ile171=
ENST00000400913.6:c.339T>C	ENSP00000383704.1:p.Ile113=
ENST00000400915.8:c.450T>C	ENSP00000383706.4:p.Ile150=
ENST00000489097.6:n.815T>C
ENST00000535355.6:c.546T>C	ENSP00000441445.1:p.Ile182=
ENST00000537245.6:c.450T>C	ENSP00000439625.2:p.Ile150=
ENST00000673471.2:c.636T>C	ENSP00000500749.1:p.Ile212=
ENST00000674790.1:c.*551T>C	ENSP00000502815.1:n.*551T>C
ENST00000675123.1:c.339T>C	ENSP00000502132.1:p.Ile113=
ENST00000675548.1:c.*167T>C	ENSP00000502684.1:n.*167T>C
ENST00000675694.1:c.339T>C	ENSP00000501925.1:p.Ile113=
ENST00000676255.1:c.301T>C	ENSP00000502459.1:n.301T>C
ENST00000340850.9:c.339T>C	ENSP00000344570.5:p.Ile113=
ENST00000377725.5:c.339T>C	ENSP00000366954.1:p.Ile113=
ENST00000377728.7:c.339T>C	ENSP00000366957.3:p.Ile113=
ENST00000377732.5:c.450T>C	ENSP00000366961.1:p.Ile150=
ENST00000377740.4:c.570T>C	ENSP00000366969.3:p.Ile190=
ENST00000377748.5:c.570T>C	ENSP00000366977.1:p.Ile190=
ENST00000400913.5:c.339T>C	ENSP00000383704.1:p.Ile113=
ENST00000400915.7:c.507T>C	ENSP00000383706.3:p.Ile169=
ENST00000489097.5:n.815T>C
ENST00000535355.5:c.546T>C	ENSP00000441445.1:p.Ile182=
ENST00000537245.5:c.576T>C	ENSP00000439625.1:p.Ile192=
NM_001042663.1:c.507T>C	NP_001036128.1:p.Ile169=
NM_001042664.1:c.339T>C	NP_001036129.1:p.Ile113=
NM_001042665.1:c.339T>C	NP_001036130.1:p.Ile113=
NM_001265592.1:c.576T>C	NP_001252521.1:p.Ile192=
NM_001265593.1:c.546T>C	NP_001252522.1:p.Ile182=
NM_001265594.1:c.339T>C	NP_001252523.1:p.Ile113=
NM_020631.4:c.339T>C	NP_065682.2:p.Ile113=
NM_198681.3:c.570T>C	NP_941374.2:p.Ile190=
NM_001042663.2:c.507T>C	NP_001036128.1:p.Ile169=
NM_001265594.2:c.339T>C	NP_001252523.1:p.Ile113=
NM_020631.5:c.339T>C	NP_065682.2:p.Ile113=
NM_001042663.3:c.450T>C	NP_001036128.2:p.Ile150=
NM_001265592.2:c.450T>C	NP_001252521.2:p.Ile150=
NM_020631.6:c.339T>C MANE Select	NP_065682.2:p.Ile113=
NM_198681.4:c.339T>C	NP_941374.3:p.Ile113=