Canonical Allele Identifier: CA2043057040
Gene: GRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66455102_66455108delinsAAAAATC , CM000674.2:g.66455102_66455108delinsAAAAATC GRCh38
NC_000012.11:g.66848882_66848888delinsAAAAATC , CM000674.1:g.66848882_66848888delinsAAAAATC GRCh37
NC_000012.10:g.65135149_65135155delinsAAAAATC NCBI36
NG_021400.1:g.229038_229044delinsGATTTTT
NG_021400.2:g.619158_619164delinsGATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696989.1:c.1423+301_1423+307delinsGATTTTT ENSP00000513025.1:n.1423+301_1423+307delinsGATTTTT
ENST00000359742.9:c.1354+301_1354+307delinsGATTTTT MANE Select ENSP00000352780.4:n.1354+301_1354+307delinsGATTTTT
ENST00000359742.8:c.1354+301_1354+307delinsGATTTTT ENSP00000352780.4:n.1354+301_1354+307delinsGATTTTT
ENST00000398016.7:c.1198+301_1198+307delinsGATTTTT ENSP00000381098.3:n.1198+301_1198+307delinsGATTTTT
ENST00000535002.1:c.460+301_460+307delinsGATTTTT
ENST00000536215.5:c.874+7816_874+7822delinsGATTTTT ENSP00000446011.1:n.874+7816_874+7822delinsGATTTTT
ENST00000538164.5:c.798+301_798+307delinsGATTTTT
ENST00000538211.5:c.1198+301_1198+307delinsGATTTTT ENSP00000446047.1:n.1198+301_1198+307delinsGATTTTT
ENST00000540433.5:c.1030+301_1030+307delinsGATTTTT ENSP00000446024.1:n.1030+301_1030+307delinsGATTTTT
ENST00000540854.5:c.337+60511_337+60517delinsGATTTTT ENSP00000443006.1:n.337+60511_337+60517delinsGATTTTT
ENST00000543172.5:c.656+301_656+307delinsGATTTTT
NM_001178074.1:c.1198+301_1198+307delinsGATTTTT NP_001171545.1:n.1198+301_1198+307delinsGATTTTT
NM_021150.3:c.1198+301_1198+307delinsGATTTTT NP_066973.2:n.1198+301_1198+307delinsGATTTTT
XM_005268754.3:c.1357+301_1357+307delinsGATTTTT XP_005268811.1:n.1357+301_1357+307delinsGATTTTT
XM_005268757.3:c.1276+301_1276+307delinsGATTTTT XP_005268814.1:n.1276+301_1276+307delinsGATTTTT
XM_011538089.1:c.1579+301_1579+307delinsGATTTTT XP_011536391.1:n.1579+301_1579+307delinsGATTTTT
XM_011538090.1:c.1579+301_1579+307delinsGATTTTT XP_011536392.1:n.1579+301_1579+307delinsGATTTTT
XM_011538091.1:c.1423+301_1423+307delinsGATTTTT XP_011536393.1:n.1423+301_1423+307delinsGATTTTT
XM_011538092.1:c.1423+301_1423+307delinsGATTTTT XP_011536394.1:n.1423+301_1423+307delinsGATTTTT
XM_011538093.1:c.1354+301_1354+307delinsGATTTTT XP_011536395.1:n.1354+301_1354+307delinsGATTTTT
XM_011538094.1:c.1186+301_1186+307delinsGATTTTT XP_011536396.1:n.1186+301_1186+307delinsGATTTTT
NM_001366722.1:c.1354+301_1354+307delinsGATTTTT MANE Select NP_001353651.1:n.1354+301_1354+307delinsGATTTTT
NM_001366723.1:c.1273+301_1273+307delinsGATTTTT NP_001353652.1:n.1273+301_1273+307delinsGATTTTT
NM_001366724.1:c.1276+301_1276+307delinsGATTTTT NP_001353653.1:n.1276+301_1276+307delinsGATTTTT
XM_005268754.4:c.1357+301_1357+307delinsGATTTTT XP_005268811.1:n.1357+301_1357+307delinsGATTTTT
XM_005268757.4:c.1276+301_1276+307delinsGATTTTT XP_005268814.1:n.1276+301_1276+307delinsGATTTTT
XM_017019098.1:c.1579+301_1579+307delinsGATTTTT XP_016874587.1:n.1579+301_1579+307delinsGATTTTT
XM_017019099.1:c.1432+301_1432+307delinsGATTTTT XP_016874588.1:n.1432+301_1432+307delinsGATTTTT
XM_017019100.1:c.1423+301_1423+307delinsGATTTTT XP_016874589.1:n.1423+301_1423+307delinsGATTTTT
NM_001178074.2:c.1198+301_1198+307delinsGATTTTT NP_001171545.1:n.1198+301_1198+307delinsGATTTTT
NM_021150.4:c.1198+301_1198+307delinsGATTTTT NP_066973.2:n.1198+301_1198+307delinsGATTTTT
NM_001379345.1:c.1432+301_1432+307delinsGATTTTT NP_001366274.1:n.1432+301_1432+307delinsGATTTTT
NM_001379346.1:c.1354+301_1354+307delinsGATTTTT NP_001366275.1:n.1354+301_1354+307delinsGATTTTT
NM_001379347.1:c.1276+301_1276+307delinsGATTTTT NP_001366276.1:n.1276+301_1276+307delinsGATTTTT
NM_001379348.1:c.1273+301_1273+307delinsGATTTTT NP_001366277.1:n.1273+301_1273+307delinsGATTTTT
NM_001379349.1:c.1201+301_1201+307delinsGATTTTT NP_001366278.1:n.1201+301_1201+307delinsGATTTTT
NM_001379351.1:c.1198+301_1198+307delinsGATTTTT NP_001366280.1:n.1198+301_1198+307delinsGATTTTT