Canonical Allele Identifier: CA2043057229
Gene: GRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66455545G= , CM000674.2:g.66455545G= GRCh38
NC_000012.11:g.66849325G= , CM000674.1:g.66849325G= GRCh37
NC_000012.10:g.65135592G= NCBI36
NG_021400.1:g.228601C=
NG_021400.2:g.618721C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696989.1:c.1287C= ENSP00000513025.1:p.Ser429=
ENST00000359742.9:c.1218C= MANE Select ENSP00000352780.4:p.Ser406=
ENST00000359742.8:c.1218C= ENSP00000352780.4:p.Ser406=
ENST00000398016.7:c.1062C= ENSP00000381098.3:p.Ser354=
ENST00000535002.1:c.324C=
ENST00000536215.5:c.874+7379C= ENSP00000446011.1:n.874+7379C=
ENST00000538164.5:c.662C=
ENST00000538211.5:c.1062C= ENSP00000446047.1:p.Ser354=
ENST00000540433.5:c.894C= ENSP00000446024.1:p.Ser298=
ENST00000540854.5:c.337+60074C= ENSP00000443006.1:n.337+60074C=
ENST00000543172.5:c.520C=
NM_001178074.1:c.1062C= NP_001171545.1:p.Ser354=
NM_021150.3:c.1062C= NP_066973.2:p.Ser354=
XM_005268754.3:c.1221C= XP_005268811.1:p.Ser407=
XM_005268757.3:c.1140C= XP_005268814.1:p.Ser380=
XM_011538089.1:c.1443C= XP_011536391.1:p.Ser481=
XM_011538090.1:c.1443C= XP_011536392.1:p.Ser481=
XM_011538091.1:c.1287C= XP_011536393.1:p.Ser429=
XM_011538092.1:c.1287C= XP_011536394.1:p.Ser429=
XM_011538093.1:c.1218C= XP_011536395.1:p.Ser406=
XM_011538094.1:c.1050C= XP_011536396.1:p.Ser350=
NM_001366722.1:c.1218C= MANE Select NP_001353651.1:p.Ser406=
NM_001366723.1:c.1137C= NP_001353652.1:p.Ser379=
NM_001366724.1:c.1140C= NP_001353653.1:p.Ser380=
XM_005268754.4:c.1221C= XP_005268811.1:p.Ser407=
XM_005268757.4:c.1140C= XP_005268814.1:p.Ser380=
XM_017019098.1:c.1443C= XP_016874587.1:p.Ser481=
XM_017019099.1:c.1296C= XP_016874588.1:p.Ser432=
XM_017019100.1:c.1287C= XP_016874589.1:p.Ser429=
NM_001178074.2:c.1062C= NP_001171545.1:p.Ser354=
NM_021150.4:c.1062C= NP_066973.2:p.Ser354=
NM_001379345.1:c.1296C= NP_001366274.1:p.Ser432=
NM_001379346.1:c.1218C= NP_001366275.1:p.Ser406=
NM_001379347.1:c.1140C= NP_001366276.1:p.Ser380=
NM_001379348.1:c.1137C= NP_001366277.1:p.Ser379=
NM_001379349.1:c.1065C= NP_001366278.1:p.Ser355=
NM_001379351.1:c.1062C= NP_001366280.1:p.Ser354=