Canonical Allele Identifier: CA1672598731
Gene: PLEKHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150839859T= , CM000668.2:g.150839859T= GRCh38
NC_000006.11:g.151160995T= , CM000668.1:g.151160995T= GRCh37
NC_000006.10:g.151202688T= NCBI36
NG_051299.1:g.244997T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696526.1:c.3121T= MANE Select ENSP00000512689.1:p.Leu1041=
ENST00000644968.1:c.3121T= ENSP00000496254.1:p.Leu1041=
ENST00000358517.6:c.3121T= ENSP00000351318.2:p.Leu1041=
ENST00000367328.5:c.3121T= ENSP00000356297.1:p.Leu1041=
ENST00000475490.1:c.1158-1176T= ENSP00000433107.1:n.1158-1176T=
NM_001029884.1:c.3121T= NP_001025055.1:p.Leu1041=
XM_005267064.2:c.3298T= XP_005267121.1:p.Leu1100=
XM_005267065.2:c.3121T= XP_005267122.1:p.Leu1041=
XM_005267066.1:c.3121T= XP_005267123.1:p.Leu1041=
XM_006715521.1:c.3121T= XP_006715584.1:p.Leu1041=
XM_006715522.2:c.3121T= XP_006715585.1:p.Leu1041=
XM_011535981.1:c.3337T= XP_011534283.1:p.Leu1113=
XM_011535982.1:c.3298T= XP_011534284.1:p.Leu1100=
XM_011535983.1:c.3121T= XP_011534285.1:p.Leu1041=
NM_001029884.2:c.3121T= NP_001025055.1:p.Leu1041=
NM_001329798.1:c.3298T= NP_001316727.1:p.Leu1100=
NM_001329799.1:c.3241T= NP_001316728.1:p.Leu1081=
NM_001329800.1:c.3121T= NP_001316729.1:p.Leu1041=
NM_001329801.1:c.3121T= NP_001316730.1:p.Leu1041=
NM_001329802.1:c.3082T= NP_001316731.1:p.Leu1028=
NM_001329803.1:c.3004T= NP_001316732.1:p.Leu1002=
NM_001329804.1:c.1617-1176T= NP_001316733.1:n.1617-1176T=
NM_001329805.1:c.1617-1176T= NP_001316734.1:n.1617-1176T=
NM_001329806.1:c.1617-1176T= NP_001316735.1:n.1617-1176T=
NM_001029884.3:c.3121T= MANE Select NP_001025055.1:p.Leu1041=
NM_001329798.2:c.3298T= NP_001316727.1:p.Leu1100=
NM_001329799.2:c.3241T= NP_001316728.1:p.Leu1081=
NM_001329800.2:c.3121T= NP_001316729.1:p.Leu1041=
NM_001329801.2:c.3121T= NP_001316730.1:p.Leu1041=
NM_001329802.2:c.3082T= NP_001316731.1:p.Leu1028=
NM_001329803.2:c.3004T= NP_001316732.1:p.Leu1002=
NM_001329804.2:c.1617-1176T= NP_001316733.1:n.1617-1176T=
NM_001329805.2:c.1617-1176T= NP_001316734.1:n.1617-1176T=
NM_001329806.2:c.1617-1176T= NP_001316735.1:n.1617-1176T=