Canonical Allele Identifier: CA366050798

Gene: PLEKHG1

Linked Data

• dbSNP Id: rs1489478387
• gnomAD v3: 6-150839982-G-T
• gnomAD v4: 6-150839982-G-T
• MyVariant Identifiers: chr6:g.151161118G>T (hg19) ; chr6:g.150839982G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150839982G>T , CM000668.2:g.150839982G>T	GRCh38
NC_000006.11:g.151161118G>T , CM000668.1:g.151161118G>T	GRCh37
NC_000006.10:g.151202811G>T	NCBI36
NG_051299.1:g.245120G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696526.1:c.3244G>T MANE Select	ENSP00000512689.1:p.Asp1082Tyr
ENST00000644968.1:c.3244G>T	ENSP00000496254.1:p.Asp1082Tyr
ENST00000358517.6:c.3244G>T	ENSP00000351318.2:p.Asp1082Tyr
ENST00000367328.5:c.3244G>T	ENSP00000356297.1:p.Asp1082Tyr
ENST00000475490.1:c.1158-1053G>T	ENSP00000433107.1:n.1158-1053G>T
NM_001029884.1:c.3244G>T	NP_001025055.1:p.Asp1082Tyr
XM_005267064.2:c.3421G>T	XP_005267121.1:p.Asp1141Tyr
XM_005267065.2:c.3244G>T	XP_005267122.1:p.Asp1082Tyr
XM_005267066.1:c.3244G>T	XP_005267123.1:p.Asp1082Tyr
XM_006715521.1:c.3244G>T	XP_006715584.1:p.Asp1082Tyr
XM_006715522.2:c.3244G>T	XP_006715585.1:p.Asp1082Tyr
XM_011535981.1:c.3460G>T	XP_011534283.1:p.Asp1154Tyr
XM_011535982.1:c.3421G>T	XP_011534284.1:p.Asp1141Tyr
XM_011535983.1:c.3244G>T	XP_011534285.1:p.Asp1082Tyr
NM_001029884.2:c.3244G>T	NP_001025055.1:p.Asp1082Tyr
NM_001329798.1:c.3421G>T	NP_001316727.1:p.Asp1141Tyr
NM_001329799.1:c.3364G>T	NP_001316728.1:p.Asp1122Tyr
NM_001329800.1:c.3244G>T	NP_001316729.1:p.Asp1082Tyr
NM_001329801.1:c.3244G>T	NP_001316730.1:p.Asp1082Tyr
NM_001329802.1:c.3205G>T	NP_001316731.1:p.Asp1069Tyr
NM_001329803.1:c.3127G>T	NP_001316732.1:p.Asp1043Tyr
NM_001329804.1:c.1617-1053G>T	NP_001316733.1:n.1617-1053G>T
NM_001329805.1:c.1617-1053G>T	NP_001316734.1:n.1617-1053G>T
NM_001329806.1:c.1617-1053G>T	NP_001316735.1:n.1617-1053G>T
NM_001029884.3:c.3244G>T MANE Select	NP_001025055.1:p.Asp1082Tyr
NM_001329798.2:c.3421G>T	NP_001316727.1:p.Asp1141Tyr
NM_001329799.2:c.3364G>T	NP_001316728.1:p.Asp1122Tyr
NM_001329800.2:c.3244G>T	NP_001316729.1:p.Asp1082Tyr
NM_001329801.2:c.3244G>T	NP_001316730.1:p.Asp1082Tyr
NM_001329802.2:c.3205G>T	NP_001316731.1:p.Asp1069Tyr
NM_001329803.2:c.3127G>T	NP_001316732.1:p.Asp1043Tyr
NM_001329804.2:c.1617-1053G>T	NP_001316733.1:n.1617-1053G>T
NM_001329805.2:c.1617-1053G>T	NP_001316734.1:n.1617-1053G>T
NM_001329806.2:c.1617-1053G>T	NP_001316735.1:n.1617-1053G>T