Canonical Allele Identifier: CA521018449

Gene: PLEKHG5

Linked Data

• dbSNP Id: rs1380123640
• gnomAD v2: 1-6529531-TCAGTGTCAG-T
• MyVariant Identifiers: chr1:g.6529532_6529540del (hg19) ; chr1:g.6469472_6469480del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469475_6469483del , CM000663.2:g.6469475_6469483del	GRCh38
NC_000001.10:g.6529535_6529543del , CM000663.1:g.6529535_6529543del	GRCh37
NC_000001.9:g.6452122_6452130del	NCBI36
NG_007978.1:g.55530_55538del , LRG_262:g.55530_55538del
NG_029910.1:g.1716_1724del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1934-30_1934-22del	ENSP00000344570.5:n.1934-30_1934-22del
ENST00000377728.8:c.1934-30_1934-22del MANE Select	ENSP00000366957.3:n.1934-30_1934-22del
ENST00000377740.5:c.1934-30_1934-22del	ENSP00000366969.4:n.1934-30_1934-22del
ENST00000377748.6:c.2108-30_2108-22del	ENSP00000366977.2:n.2108-30_2108-22del
ENST00000400913.6:c.1934-30_1934-22del	ENSP00000383704.1:n.1934-30_1934-22del
ENST00000400915.8:c.2045-30_2045-22del	ENSP00000383706.4:n.2045-30_2045-22del
ENST00000489097.6:n.2410-30_2410-22del
ENST00000535355.6:c.2141-30_2141-22del	ENSP00000441445.1:n.2141-30_2141-22del
ENST00000537245.6:c.2045-30_2045-22del	ENSP00000439625.2:n.2045-30_2045-22del
ENST00000673471.2:c.2231-30_2231-22del	ENSP00000500749.1:n.2231-30_2231-22del
ENST00000674790.1:c.*2146-30_*2146-22del	ENSP00000502815.1:n.*2146-30_*2146-22del
ENST00000675123.1:c.1934-30_1934-22del	ENSP00000502132.1:n.1934-30_1934-22del
ENST00000675548.1:c.*1762-30_*1762-22del	ENSP00000502684.1:n.*1762-30_*1762-22del
ENST00000675694.1:c.1934-30_1934-22del	ENSP00000501925.1:n.1934-30_1934-22del
ENST00000676401.1:n.481-30_481-22del
ENST00000340850.9:c.1934-30_1934-22del	ENSP00000344570.5:n.1934-30_1934-22del
ENST00000377725.5:c.1934-30_1934-22del	ENSP00000366954.1:n.1934-30_1934-22del
ENST00000377728.7:c.1934-30_1934-22del	ENSP00000366957.3:n.1934-30_1934-22del
ENST00000377732.5:c.2045-30_2045-22del	ENSP00000366961.1:n.2045-30_2045-22del
ENST00000377740.4:c.2165-30_2165-22del	ENSP00000366969.3:n.2165-30_2165-22del
ENST00000377748.5:c.2165-30_2165-22del	ENSP00000366977.1:n.2165-30_2165-22del
ENST00000400913.5:c.1934-30_1934-22del	ENSP00000383704.1:n.1934-30_1934-22del
ENST00000400915.7:c.2102-30_2102-22del	ENSP00000383706.3:n.2102-30_2102-22del
ENST00000487949.4:n.1136-30_1136-22del
ENST00000489097.5:n.2410-30_2410-22del
ENST00000535355.5:c.2141-30_2141-22del	ENSP00000441445.1:n.2141-30_2141-22del
ENST00000537245.5:c.2171-30_2171-22del	ENSP00000439625.1:n.2171-30_2171-22del
NM_001042663.1:c.2102-30_2102-22del	NP_001036128.1:n.2102-30_2102-22del
NM_001042664.1:c.1934-30_1934-22del	NP_001036129.1:n.1934-30_1934-22del
NM_001042665.1:c.1934-30_1934-22del	NP_001036130.1:n.1934-30_1934-22del
NM_001265592.1:c.2171-30_2171-22del	NP_001252521.1:n.2171-30_2171-22del
NM_001265593.1:c.2141-30_2141-22del	NP_001252522.1:n.2141-30_2141-22del
NM_001265594.1:c.1934-30_1934-22del	NP_001252523.1:n.1934-30_1934-22del
NM_020631.4:c.1934-30_1934-22del	NP_065682.2:n.1934-30_1934-22del
NM_198681.3:c.2165-30_2165-22del	NP_941374.2:n.2165-30_2165-22del
NM_001042663.2:c.2102-30_2102-22del	NP_001036128.1:n.2102-30_2102-22del
NM_001265594.2:c.1934-30_1934-22del	NP_001252523.1:n.1934-30_1934-22del
NM_020631.5:c.1934-30_1934-22del	NP_065682.2:n.1934-30_1934-22del
NM_001042663.3:c.2045-30_2045-22del	NP_001036128.2:n.2045-30_2045-22del
NM_001265592.2:c.2045-30_2045-22del	NP_001252521.2:n.2045-30_2045-22del
NM_020631.6:c.1934-30_1934-22del MANE Select	NP_065682.2:n.1934-30_1934-22del
NM_198681.4:c.1934-30_1934-22del	NP_941374.3:n.1934-30_1934-22del