Canonical Allele Identifier: CA2043057006

Gene: GRIP1

Linked Data

• dbSNP Id: rs2058916156

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455030_66455033dup , CM000674.2:g.66455030_66455033dup	GRCh38
NC_000012.11:g.66848810_66848813dup , CM000674.1:g.66848810_66848813dup	GRCh37
NC_000012.10:g.65135077_65135080dup	NCBI36
NG_021400.1:g.229115_229118dup
NG_021400.2:g.619235_619238dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696989.1:c.1423+378_1423+381dup	ENSP00000513025.1:n.1423+378_1423+381dup
ENST00000359742.9:c.1354+378_1354+381dup MANE Select	ENSP00000352780.4:n.1354+378_1354+381dup
ENST00000359742.8:c.1354+378_1354+381dup	ENSP00000352780.4:n.1354+378_1354+381dup
ENST00000398016.7:c.1198+378_1198+381dup	ENSP00000381098.3:n.1198+378_1198+381dup
ENST00000535002.1:c.460+378_460+381dup
ENST00000536215.5:c.874+7893_874+7896dup	ENSP00000446011.1:n.874+7893_874+7896dup
ENST00000538164.5:c.798+378_798+381dup
ENST00000538211.5:c.1198+378_1198+381dup	ENSP00000446047.1:n.1198+378_1198+381dup
ENST00000540433.5:c.1030+378_1030+381dup	ENSP00000446024.1:n.1030+378_1030+381dup
ENST00000540854.5:c.337+60588_337+60591dup	ENSP00000443006.1:n.337+60588_337+60591dup
ENST00000543172.5:c.656+378_656+381dup
NM_001178074.1:c.1198+378_1198+381dup	NP_001171545.1:n.1198+378_1198+381dup
NM_021150.3:c.1198+378_1198+381dup	NP_066973.2:n.1198+378_1198+381dup
XM_005268754.3:c.1357+378_1357+381dup	XP_005268811.1:n.1357+378_1357+381dup
XM_005268757.3:c.1276+378_1276+381dup	XP_005268814.1:n.1276+378_1276+381dup
XM_011538089.1:c.1579+378_1579+381dup	XP_011536391.1:n.1579+378_1579+381dup
XM_011538090.1:c.1579+378_1579+381dup	XP_011536392.1:n.1579+378_1579+381dup
XM_011538091.1:c.1423+378_1423+381dup	XP_011536393.1:n.1423+378_1423+381dup
XM_011538092.1:c.1423+378_1423+381dup	XP_011536394.1:n.1423+378_1423+381dup
XM_011538093.1:c.1354+378_1354+381dup	XP_011536395.1:n.1354+378_1354+381dup
XM_011538094.1:c.1186+378_1186+381dup	XP_011536396.1:n.1186+378_1186+381dup
NM_001366722.1:c.1354+378_1354+381dup MANE Select	NP_001353651.1:n.1354+378_1354+381dup
NM_001366723.1:c.1273+378_1273+381dup	NP_001353652.1:n.1273+378_1273+381dup
NM_001366724.1:c.1276+378_1276+381dup	NP_001353653.1:n.1276+378_1276+381dup
XM_005268754.4:c.1357+378_1357+381dup	XP_005268811.1:n.1357+378_1357+381dup
XM_005268757.4:c.1276+378_1276+381dup	XP_005268814.1:n.1276+378_1276+381dup
XM_017019098.1:c.1579+378_1579+381dup	XP_016874587.1:n.1579+378_1579+381dup
XM_017019099.1:c.1432+378_1432+381dup	XP_016874588.1:n.1432+378_1432+381dup
XM_017019100.1:c.1423+378_1423+381dup	XP_016874589.1:n.1423+378_1423+381dup
NM_001178074.2:c.1198+378_1198+381dup	NP_001171545.1:n.1198+378_1198+381dup
NM_021150.4:c.1198+378_1198+381dup	NP_066973.2:n.1198+378_1198+381dup
NM_001379345.1:c.1432+378_1432+381dup	NP_001366274.1:n.1432+378_1432+381dup
NM_001379346.1:c.1354+378_1354+381dup	NP_001366275.1:n.1354+378_1354+381dup
NM_001379347.1:c.1276+378_1276+381dup	NP_001366276.1:n.1276+378_1276+381dup
NM_001379348.1:c.1273+378_1273+381dup	NP_001366277.1:n.1273+378_1273+381dup
NM_001379349.1:c.1201+378_1201+381dup	NP_001366278.1:n.1201+378_1201+381dup
NM_001379351.1:c.1198+378_1198+381dup	NP_001366280.1:n.1198+378_1198+381dup