Canonical Allele Identifier: CA2043057056
Gene: GRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.66455133_66455134delinsCA , CM000674.2:g.66455133_66455134delinsCA GRCh38
NC_000012.11:g.66848913_66848914delinsCA , CM000674.1:g.66848913_66848914delinsCA GRCh37
NC_000012.10:g.65135180_65135181delinsCA NCBI36
NG_021400.1:g.229012_229013delinsTG
NG_021400.2:g.619132_619133delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696989.1:c.1423+275_1423+276delinsTG ENSP00000513025.1:n.1423+275_1423+276delinsTG
ENST00000359742.9:c.1354+275_1354+276delinsTG MANE Select ENSP00000352780.4:n.1354+275_1354+276delinsTG
ENST00000359742.8:c.1354+275_1354+276delinsTG ENSP00000352780.4:n.1354+275_1354+276delinsTG
ENST00000398016.7:c.1198+275_1198+276delinsTG ENSP00000381098.3:n.1198+275_1198+276delinsTG
ENST00000535002.1:c.460+275_460+276delinsTG
ENST00000536215.5:c.874+7790_874+7791delinsTG ENSP00000446011.1:n.874+7790_874+7791delinsTG
ENST00000538164.5:c.798+275_798+276delinsTG
ENST00000538211.5:c.1198+275_1198+276delinsTG ENSP00000446047.1:n.1198+275_1198+276delinsTG
ENST00000540433.5:c.1030+275_1030+276delinsTG ENSP00000446024.1:n.1030+275_1030+276delinsTG
ENST00000540854.5:c.337+60485_337+60486delinsTG ENSP00000443006.1:n.337+60485_337+60486delinsTG
ENST00000543172.5:c.656+275_656+276delinsTG
NM_001178074.1:c.1198+275_1198+276delinsTG NP_001171545.1:n.1198+275_1198+276delinsTG
NM_021150.3:c.1198+275_1198+276delinsTG NP_066973.2:n.1198+275_1198+276delinsTG
XM_005268754.3:c.1357+275_1357+276delinsTG XP_005268811.1:n.1357+275_1357+276delinsTG
XM_005268757.3:c.1276+275_1276+276delinsTG XP_005268814.1:n.1276+275_1276+276delinsTG
XM_011538089.1:c.1579+275_1579+276delinsTG XP_011536391.1:n.1579+275_1579+276delinsTG
XM_011538090.1:c.1579+275_1579+276delinsTG XP_011536392.1:n.1579+275_1579+276delinsTG
XM_011538091.1:c.1423+275_1423+276delinsTG XP_011536393.1:n.1423+275_1423+276delinsTG
XM_011538092.1:c.1423+275_1423+276delinsTG XP_011536394.1:n.1423+275_1423+276delinsTG
XM_011538093.1:c.1354+275_1354+276delinsTG XP_011536395.1:n.1354+275_1354+276delinsTG
XM_011538094.1:c.1186+275_1186+276delinsTG XP_011536396.1:n.1186+275_1186+276delinsTG
NM_001366722.1:c.1354+275_1354+276delinsTG MANE Select NP_001353651.1:n.1354+275_1354+276delinsTG
NM_001366723.1:c.1273+275_1273+276delinsTG NP_001353652.1:n.1273+275_1273+276delinsTG
NM_001366724.1:c.1276+275_1276+276delinsTG NP_001353653.1:n.1276+275_1276+276delinsTG
XM_005268754.4:c.1357+275_1357+276delinsTG XP_005268811.1:n.1357+275_1357+276delinsTG
XM_005268757.4:c.1276+275_1276+276delinsTG XP_005268814.1:n.1276+275_1276+276delinsTG
XM_017019098.1:c.1579+275_1579+276delinsTG XP_016874587.1:n.1579+275_1579+276delinsTG
XM_017019099.1:c.1432+275_1432+276delinsTG XP_016874588.1:n.1432+275_1432+276delinsTG
XM_017019100.1:c.1423+275_1423+276delinsTG XP_016874589.1:n.1423+275_1423+276delinsTG
NM_001178074.2:c.1198+275_1198+276delinsTG NP_001171545.1:n.1198+275_1198+276delinsTG
NM_021150.4:c.1198+275_1198+276delinsTG NP_066973.2:n.1198+275_1198+276delinsTG
NM_001379345.1:c.1432+275_1432+276delinsTG NP_001366274.1:n.1432+275_1432+276delinsTG
NM_001379346.1:c.1354+275_1354+276delinsTG NP_001366275.1:n.1354+275_1354+276delinsTG
NM_001379347.1:c.1276+275_1276+276delinsTG NP_001366276.1:n.1276+275_1276+276delinsTG
NM_001379348.1:c.1273+275_1273+276delinsTG NP_001366277.1:n.1273+275_1273+276delinsTG
NM_001379349.1:c.1201+275_1201+276delinsTG NP_001366278.1:n.1201+275_1201+276delinsTG
NM_001379351.1:c.1198+275_1198+276delinsTG NP_001366280.1:n.1198+275_1198+276delinsTG