Canonical Allele Identifier: CA2043057207
Gene: GRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66455490G= , CM000674.2:g.66455490G= GRCh38
NC_000012.11:g.66849270G= , CM000674.1:g.66849270G= GRCh37
NC_000012.10:g.65135537G= NCBI36
NG_021400.1:g.228656C=
NG_021400.2:g.618776C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696989.1:c.1342C= ENSP00000513025.1:p.Leu448=
ENST00000359742.9:c.1273C= MANE Select ENSP00000352780.4:p.Leu425=
ENST00000359742.8:c.1273C= ENSP00000352780.4:p.Leu425=
ENST00000398016.7:c.1117C= ENSP00000381098.3:p.Leu373=
ENST00000535002.1:c.379C=
ENST00000536215.5:c.874+7434C= ENSP00000446011.1:n.874+7434C=
ENST00000538164.5:c.717C=
ENST00000538211.5:c.1117C= ENSP00000446047.1:p.Leu373=
ENST00000540433.5:c.949C= ENSP00000446024.1:p.Leu317=
ENST00000540854.5:c.337+60129C= ENSP00000443006.1:n.337+60129C=
ENST00000543172.5:c.575C=
NM_001178074.1:c.1117C= NP_001171545.1:p.Leu373=
NM_021150.3:c.1117C= NP_066973.2:p.Leu373=
XM_005268754.3:c.1276C= XP_005268811.1:p.Leu426=
XM_005268757.3:c.1195C= XP_005268814.1:p.Leu399=
XM_011538089.1:c.1498C= XP_011536391.1:p.Leu500=
XM_011538090.1:c.1498C= XP_011536392.1:p.Leu500=
XM_011538091.1:c.1342C= XP_011536393.1:p.Leu448=
XM_011538092.1:c.1342C= XP_011536394.1:p.Leu448=
XM_011538093.1:c.1273C= XP_011536395.1:p.Leu425=
XM_011538094.1:c.1105C= XP_011536396.1:p.Leu369=
NM_001366722.1:c.1273C= MANE Select NP_001353651.1:p.Leu425=
NM_001366723.1:c.1192C= NP_001353652.1:p.Leu398=
NM_001366724.1:c.1195C= NP_001353653.1:p.Leu399=
XM_005268754.4:c.1276C= XP_005268811.1:p.Leu426=
XM_005268757.4:c.1195C= XP_005268814.1:p.Leu399=
XM_017019098.1:c.1498C= XP_016874587.1:p.Leu500=
XM_017019099.1:c.1351C= XP_016874588.1:p.Leu451=
XM_017019100.1:c.1342C= XP_016874589.1:p.Leu448=
NM_001178074.2:c.1117C= NP_001171545.1:p.Leu373=
NM_021150.4:c.1117C= NP_066973.2:p.Leu373=
NM_001379345.1:c.1351C= NP_001366274.1:p.Leu451=
NM_001379346.1:c.1273C= NP_001366275.1:p.Leu425=
NM_001379347.1:c.1195C= NP_001366276.1:p.Leu399=
NM_001379348.1:c.1192C= NP_001366277.1:p.Leu398=
NM_001379349.1:c.1120C= NP_001366278.1:p.Leu374=
NM_001379351.1:c.1117C= NP_001366280.1:p.Leu373=