Canonical Allele Identifier: CA452725462

Gene: PLEKHG1

Linked Data

• MyVariant Identifiers: chr6:g.151160979T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150839843T>C , CM000668.2:g.150839843T>C	GRCh38
NC_000006.11:g.151160979T>C , CM000668.1:g.151160979T>C	GRCh37
NC_000006.10:g.151202672T>C	NCBI36
NG_051299.1:g.244981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696526.1:c.3105T>C MANE Select	ENSP00000512689.1:p.Ile1035=
ENST00000644968.1:c.3105T>C	ENSP00000496254.1:p.Ile1035=
ENST00000358517.6:c.3105T>C	ENSP00000351318.2:p.Ile1035=
ENST00000367328.5:c.3105T>C	ENSP00000356297.1:p.Ile1035=
ENST00000475490.1:c.1158-1192T>C	ENSP00000433107.1:n.1158-1192T>C
NM_001029884.1:c.3105T>C	NP_001025055.1:p.Ile1035=
XM_005267064.2:c.3282T>C	XP_005267121.1:p.Ile1094=
XM_005267065.2:c.3105T>C	XP_005267122.1:p.Ile1035=
XM_005267066.1:c.3105T>C	XP_005267123.1:p.Ile1035=
XM_006715521.1:c.3105T>C	XP_006715584.1:p.Ile1035=
XM_006715522.2:c.3105T>C	XP_006715585.1:p.Ile1035=
XM_011535981.1:c.3321T>C	XP_011534283.1:p.Ile1107=
XM_011535982.1:c.3282T>C	XP_011534284.1:p.Ile1094=
XM_011535983.1:c.3105T>C	XP_011534285.1:p.Ile1035=
NM_001029884.2:c.3105T>C	NP_001025055.1:p.Ile1035=
NM_001329798.1:c.3282T>C	NP_001316727.1:p.Ile1094=
NM_001329799.1:c.3225T>C	NP_001316728.1:p.Ile1075=
NM_001329800.1:c.3105T>C	NP_001316729.1:p.Ile1035=
NM_001329801.1:c.3105T>C	NP_001316730.1:p.Ile1035=
NM_001329802.1:c.3066T>C	NP_001316731.1:p.Ile1022=
NM_001329803.1:c.2988T>C	NP_001316732.1:p.Ile996=
NM_001329804.1:c.1617-1192T>C	NP_001316733.1:n.1617-1192T>C
NM_001329805.1:c.1617-1192T>C	NP_001316734.1:n.1617-1192T>C
NM_001329806.1:c.1617-1192T>C	NP_001316735.1:n.1617-1192T>C
NM_001029884.3:c.3105T>C MANE Select	NP_001025055.1:p.Ile1035=
NM_001329798.2:c.3282T>C	NP_001316727.1:p.Ile1094=
NM_001329799.2:c.3225T>C	NP_001316728.1:p.Ile1075=
NM_001329800.2:c.3105T>C	NP_001316729.1:p.Ile1035=
NM_001329801.2:c.3105T>C	NP_001316730.1:p.Ile1035=
NM_001329802.2:c.3066T>C	NP_001316731.1:p.Ile1022=
NM_001329803.2:c.2988T>C	NP_001316732.1:p.Ile996=
NM_001329804.2:c.1617-1192T>C	NP_001316733.1:n.1617-1192T>C
NM_001329805.2:c.1617-1192T>C	NP_001316734.1:n.1617-1192T>C
NM_001329806.2:c.1617-1192T>C	NP_001316735.1:n.1617-1192T>C