Canonical Allele Identifier: CA1672598742
Gene: PLEKHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150839889C= , CM000668.2:g.150839889C= GRCh38
NC_000006.11:g.151161025C= , CM000668.1:g.151161025C= GRCh37
NC_000006.10:g.151202718C= NCBI36
NG_051299.1:g.245027C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696526.1:c.3151C= MANE Select ENSP00000512689.1:p.Pro1051=
ENST00000644968.1:c.3151C= ENSP00000496254.1:p.Pro1051=
ENST00000358517.6:c.3151C= ENSP00000351318.2:p.Pro1051=
ENST00000367328.5:c.3151C= ENSP00000356297.1:p.Pro1051=
ENST00000475490.1:c.1158-1146C= ENSP00000433107.1:n.1158-1146C=
NM_001029884.1:c.3151C= NP_001025055.1:p.Pro1051=
XM_005267064.2:c.3328C= XP_005267121.1:p.Pro1110=
XM_005267065.2:c.3151C= XP_005267122.1:p.Pro1051=
XM_005267066.1:c.3151C= XP_005267123.1:p.Pro1051=
XM_006715521.1:c.3151C= XP_006715584.1:p.Pro1051=
XM_006715522.2:c.3151C= XP_006715585.1:p.Pro1051=
XM_011535981.1:c.3367C= XP_011534283.1:p.Pro1123=
XM_011535982.1:c.3328C= XP_011534284.1:p.Pro1110=
XM_011535983.1:c.3151C= XP_011534285.1:p.Pro1051=
NM_001029884.2:c.3151C= NP_001025055.1:p.Pro1051=
NM_001329798.1:c.3328C= NP_001316727.1:p.Pro1110=
NM_001329799.1:c.3271C= NP_001316728.1:p.Pro1091=
NM_001329800.1:c.3151C= NP_001316729.1:p.Pro1051=
NM_001329801.1:c.3151C= NP_001316730.1:p.Pro1051=
NM_001329802.1:c.3112C= NP_001316731.1:p.Pro1038=
NM_001329803.1:c.3034C= NP_001316732.1:p.Pro1012=
NM_001329804.1:c.1617-1146C= NP_001316733.1:n.1617-1146C=
NM_001329805.1:c.1617-1146C= NP_001316734.1:n.1617-1146C=
NM_001329806.1:c.1617-1146C= NP_001316735.1:n.1617-1146C=
NM_001029884.3:c.3151C= MANE Select NP_001025055.1:p.Pro1051=
NM_001329798.2:c.3328C= NP_001316727.1:p.Pro1110=
NM_001329799.2:c.3271C= NP_001316728.1:p.Pro1091=
NM_001329800.2:c.3151C= NP_001316729.1:p.Pro1051=
NM_001329801.2:c.3151C= NP_001316730.1:p.Pro1051=
NM_001329802.2:c.3112C= NP_001316731.1:p.Pro1038=
NM_001329803.2:c.3034C= NP_001316732.1:p.Pro1012=
NM_001329804.2:c.1617-1146C= NP_001316733.1:n.1617-1146C=
NM_001329805.2:c.1617-1146C= NP_001316734.1:n.1617-1146C=
NM_001329806.2:c.1617-1146C= NP_001316735.1:n.1617-1146C=