Canonical Allele Identifier: CA4048098

Gene: PLEKHG1

Linked Data

• dbSNP Id: rs751134666
• ExAC: 6:151160935 G / T
• gnomAD v2: 6-151160935-G-T
• gnomAD v4: 6-150839799-G-T
• MyVariant Identifiers: chr6:g.151160935G>T (hg19) ; chr6:g.150839799G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150839799G>T , CM000668.2:g.150839799G>T	GRCh38
NC_000006.11:g.151160935G>T , CM000668.1:g.151160935G>T	GRCh37
NC_000006.10:g.151202628G>T	NCBI36
NG_051299.1:g.244937G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696526.1:c.3095-34G>T MANE Select	ENSP00000512689.1:n.3095-34G>T
ENST00000644968.1:c.3095-34G>T	ENSP00000496254.1:n.3095-34G>T
ENST00000358517.6:c.3095-34G>T	ENSP00000351318.2:n.3095-34G>T
ENST00000367328.5:c.3095-34G>T	ENSP00000356297.1:n.3095-34G>T
ENST00000475490.1:c.1158-1236G>T	ENSP00000433107.1:n.1158-1236G>T
NM_001029884.1:c.3095-34G>T	NP_001025055.1:n.3095-34G>T
XM_005267064.2:c.3272-34G>T	XP_005267121.1:n.3272-34G>T
XM_005267065.2:c.3095-34G>T	XP_005267122.1:n.3095-34G>T
XM_005267066.1:c.3095-34G>T	XP_005267123.1:n.3095-34G>T
XM_006715521.1:c.3095-34G>T	XP_006715584.1:n.3095-34G>T
XM_006715522.2:c.3095-34G>T	XP_006715585.1:n.3095-34G>T
XM_011535981.1:c.3311-34G>T	XP_011534283.1:n.3311-34G>T
XM_011535982.1:c.3272-34G>T	XP_011534284.1:n.3272-34G>T
XM_011535983.1:c.3095-34G>T	XP_011534285.1:n.3095-34G>T
NM_001029884.2:c.3095-34G>T	NP_001025055.1:n.3095-34G>T
NM_001329798.1:c.3272-34G>T	NP_001316727.1:n.3272-34G>T
NM_001329799.1:c.3215-34G>T	NP_001316728.1:n.3215-34G>T
NM_001329800.1:c.3095-34G>T	NP_001316729.1:n.3095-34G>T
NM_001329801.1:c.3095-34G>T	NP_001316730.1:n.3095-34G>T
NM_001329802.1:c.3056-34G>T	NP_001316731.1:n.3056-34G>T
NM_001329803.1:c.2978-34G>T	NP_001316732.1:n.2978-34G>T
NM_001329804.1:c.1617-1236G>T	NP_001316733.1:n.1617-1236G>T
NM_001329805.1:c.1617-1236G>T	NP_001316734.1:n.1617-1236G>T
NM_001329806.1:c.1617-1236G>T	NP_001316735.1:n.1617-1236G>T
NM_001029884.3:c.3095-34G>T MANE Select	NP_001025055.1:n.3095-34G>T
NM_001329798.2:c.3272-34G>T	NP_001316727.1:n.3272-34G>T
NM_001329799.2:c.3215-34G>T	NP_001316728.1:n.3215-34G>T
NM_001329800.2:c.3095-34G>T	NP_001316729.1:n.3095-34G>T
NM_001329801.2:c.3095-34G>T	NP_001316730.1:n.3095-34G>T
NM_001329802.2:c.3056-34G>T	NP_001316731.1:n.3056-34G>T
NM_001329803.2:c.2978-34G>T	NP_001316732.1:n.2978-34G>T
NM_001329804.2:c.1617-1236G>T	NP_001316733.1:n.1617-1236G>T
NM_001329805.2:c.1617-1236G>T	NP_001316734.1:n.1617-1236G>T
NM_001329806.2:c.1617-1236G>T	NP_001316735.1:n.1617-1236G>T