Canonical Allele Identifier: CA385680499
Gene: GRIP1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66678883A>T , CM000674.2:g.66678883A>T GRCh38
NC_000012.11:g.67072663A>T , CM000674.1:g.67072663A>T GRCh37
NC_000012.10:g.65358930A>T NCBI36
NG_021400.1:g.5263T>A
NG_021400.2:g.395383T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359742.9:c.22T>A MANE Select ENSP00000352780.4:p.Cys8Ser
ENST00000643019.1:c.59-81956T>A ENSP00000495444.1:n.59-81956T>A
ENST00000359742.8:c.22T>A ENSP00000352780.4:p.Cys8Ser
ENST00000398016.7:c.22T>A ENSP00000381098.3:p.Cys8Ser
ENST00000538211.5:c.22T>A ENSP00000446047.1:p.Cys8Ser
ENST00000538373.1:c.-419-48547T>A ENSP00000446067.1:n.-419-48547T>A
ENST00000539540.5:c.-113-81956T>A ENSP00000443392.1:n.-113-81956T>A
ENST00000540433.5:c.-33+125049T>A ENSP00000446024.1:n.-33+125049T>A
ENST00000541947.1:c.134-81956T>A ENSP00000438921.1:n.134-81956T>A
ENST00000545666.5:c.22T>A ENSP00000439124.2:p.Cys8Ser
NM_001178074.1:c.22T>A NP_001171545.1:p.Cys8Ser
NM_021150.3:c.22T>A NP_066973.2:p.Cys8Ser
XM_005268754.3:c.59-81956T>A XP_005268811.1:n.59-81956T>A
XM_005268757.3:c.59-136933T>A XP_005268814.1:n.59-136933T>A
XM_011538093.1:c.22T>A XP_011536395.1:p.Cys8Ser
NM_001366722.1:c.22T>A MANE Select NP_001353651.1:p.Cys8Ser
NM_001366723.1:c.134-81956T>A NP_001353652.1:n.134-81956T>A
NM_001366724.1:c.134-81956T>A NP_001353653.1:n.134-81956T>A
XM_005268754.4:c.59-81956T>A XP_005268811.1:n.59-81956T>A
XM_005268757.4:c.59-136933T>A XP_005268814.1:n.59-136933T>A
XM_017019099.1:c.134-81956T>A XP_016874588.1:n.134-81956T>A
NM_001178074.2:c.22T>A NP_001171545.1:p.Cys8Ser
NM_021150.4:c.22T>A NP_066973.2:p.Cys8Ser
NM_001379345.1:c.134-81956T>A NP_001366274.1:n.134-81956T>A
NM_001379346.1:c.22T>A NP_001366275.1:p.Cys8Ser
NM_001379347.1:c.134-81956T>A NP_001366276.1:n.134-81956T>A
NM_001379348.1:c.134-81956T>A NP_001366277.1:n.134-81956T>A
NM_001379349.1:c.59-81956T>A NP_001366278.1:n.59-81956T>A
NM_001379351.1:c.59-81956T>A NP_001366280.1:n.59-81956T>A