Canonical Allele Identifier: CA416022000

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6527974T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6467914T>A , CM000663.2:g.6467914T>A	GRCh38
NC_000001.10:g.6527974T>A , CM000663.1:g.6527974T>A	GRCh37
NC_000001.9:g.6450561T>A	NCBI36
NG_007978.1:g.57096A>T , LRG_262:g.57096A>T
NG_029910.1:g.3282A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2922A>T	ENSP00000344570.5:p.Pro974=
ENST00000377728.8:c.2922A>T MANE Select	ENSP00000366957.3:p.Pro974=
ENST00000377740.5:c.2922A>T	ENSP00000366969.4:p.Pro974=
ENST00000377748.6:c.3096A>T	ENSP00000366977.2:p.Pro1032=
ENST00000400913.6:c.2922A>T	ENSP00000383704.1:p.Pro974=
ENST00000400915.8:c.3033A>T	ENSP00000383706.4:p.Pro1011=
ENST00000489097.6:n.3398A>T
ENST00000535355.6:c.3129A>T	ENSP00000441445.1:p.Pro1043=
ENST00000537245.6:c.3033A>T	ENSP00000439625.2:p.Pro1011=
ENST00000673471.2:c.3219A>T	ENSP00000500749.1:p.Pro1073=
ENST00000674790.1:c.*3134A>T	ENSP00000502815.1:n.*3134A>T
ENST00000675123.1:c.2250-21A>T	ENSP00000502132.1:n.2250-21A>T
ENST00000675548.1:c.*2750A>T	ENSP00000502684.1:n.*2750A>T
ENST00000675694.1:c.2922A>T	ENSP00000501925.1:p.Pro974=
ENST00000675976.1:c.795A>T	ENSP00000501611.1:p.Pro265=
ENST00000340850.9:c.2922A>T	ENSP00000344570.5:p.Pro974=
ENST00000377725.5:c.2738-16A>T	ENSP00000366954.1:n.2738-16A>T
ENST00000377728.7:c.2922A>T	ENSP00000366957.3:p.Pro974=
ENST00000377732.5:c.3033A>T	ENSP00000366961.1:p.Pro1011=
ENST00000377740.4:c.2481-21A>T	ENSP00000366969.3:n.2481-21A>T
ENST00000377748.5:c.3153A>T	ENSP00000366977.1:p.Pro1051=
ENST00000400913.5:c.2922A>T	ENSP00000383704.1:p.Pro974=
ENST00000400915.7:c.3090A>T	ENSP00000383706.3:p.Pro1030=
ENST00000487949.4:n.2124A>T
ENST00000489097.5:n.3398A>T
ENST00000535355.5:c.3129A>T	ENSP00000441445.1:p.Pro1043=
ENST00000537245.5:c.3159A>T	ENSP00000439625.1:p.Pro1053=
NM_001042663.1:c.3090A>T	NP_001036128.1:p.Pro1030=
NM_001042664.1:c.2922A>T	NP_001036129.1:p.Pro974=
NM_001042665.1:c.2922A>T	NP_001036130.1:p.Pro974=
NM_001265592.1:c.3159A>T	NP_001252521.1:p.Pro1053=
NM_001265593.1:c.3129A>T	NP_001252522.1:p.Pro1043=
NM_001265594.1:c.2738-16A>T	NP_001252523.1:n.2738-16A>T
NM_020631.4:c.2922A>T	NP_065682.2:p.Pro974=
NM_198681.3:c.3153A>T	NP_941374.2:p.Pro1051=
NM_001042663.2:c.3090A>T	NP_001036128.1:p.Pro1030=
NM_001265594.2:c.2738-16A>T	NP_001252523.1:n.2738-16A>T
NM_020631.5:c.2922A>T	NP_065682.2:p.Pro974=
NM_001042663.3:c.3033A>T	NP_001036128.2:p.Pro1011=
NM_001265592.2:c.3033A>T	NP_001252521.2:p.Pro1011=
NM_020631.6:c.2922A>T MANE Select	NP_065682.2:p.Pro974=
NM_198681.4:c.2922A>T	NP_941374.3:p.Pro974=