Canonical Allele Identifier: CA2043057042

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455111_66455112delinsAT , CM000674.2:g.66455111_66455112delinsAT	GRCh38
NC_000012.11:g.66848891_66848892delinsAT , CM000674.1:g.66848891_66848892delinsAT	GRCh37
NC_000012.10:g.65135158_65135159delinsAT	NCBI36
NG_021400.1:g.229034_229035delinsAT
NG_021400.2:g.619154_619155delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696989.1:c.1423+297_1423+298delinsAT	ENSP00000513025.1:n.1423+297_1423+298delinsAT
ENST00000359742.9:c.1354+297_1354+298delinsAT MANE Select	ENSP00000352780.4:n.1354+297_1354+298delinsAT
ENST00000359742.8:c.1354+297_1354+298delinsAT	ENSP00000352780.4:n.1354+297_1354+298delinsAT
ENST00000398016.7:c.1198+297_1198+298delinsAT	ENSP00000381098.3:n.1198+297_1198+298delinsAT
ENST00000535002.1:c.460+297_460+298delinsAT
ENST00000536215.5:c.874+7812_874+7813delinsAT	ENSP00000446011.1:n.874+7812_874+7813delinsAT
ENST00000538164.5:c.798+297_798+298delinsAT
ENST00000538211.5:c.1198+297_1198+298delinsAT	ENSP00000446047.1:n.1198+297_1198+298delinsAT
ENST00000540433.5:c.1030+297_1030+298delinsAT	ENSP00000446024.1:n.1030+297_1030+298delinsAT
ENST00000540854.5:c.337+60507_337+60508delinsAT	ENSP00000443006.1:n.337+60507_337+60508delinsAT
ENST00000543172.5:c.656+297_656+298delinsAT
NM_001178074.1:c.1198+297_1198+298delinsAT	NP_001171545.1:n.1198+297_1198+298delinsAT
NM_021150.3:c.1198+297_1198+298delinsAT	NP_066973.2:n.1198+297_1198+298delinsAT
XM_005268754.3:c.1357+297_1357+298delinsAT	XP_005268811.1:n.1357+297_1357+298delinsAT
XM_005268757.3:c.1276+297_1276+298delinsAT	XP_005268814.1:n.1276+297_1276+298delinsAT
XM_011538089.1:c.1579+297_1579+298delinsAT	XP_011536391.1:n.1579+297_1579+298delinsAT
XM_011538090.1:c.1579+297_1579+298delinsAT	XP_011536392.1:n.1579+297_1579+298delinsAT
XM_011538091.1:c.1423+297_1423+298delinsAT	XP_011536393.1:n.1423+297_1423+298delinsAT
XM_011538092.1:c.1423+297_1423+298delinsAT	XP_011536394.1:n.1423+297_1423+298delinsAT
XM_011538093.1:c.1354+297_1354+298delinsAT	XP_011536395.1:n.1354+297_1354+298delinsAT
XM_011538094.1:c.1186+297_1186+298delinsAT	XP_011536396.1:n.1186+297_1186+298delinsAT
NM_001366722.1:c.1354+297_1354+298delinsAT MANE Select	NP_001353651.1:n.1354+297_1354+298delinsAT
NM_001366723.1:c.1273+297_1273+298delinsAT	NP_001353652.1:n.1273+297_1273+298delinsAT
NM_001366724.1:c.1276+297_1276+298delinsAT	NP_001353653.1:n.1276+297_1276+298delinsAT
XM_005268754.4:c.1357+297_1357+298delinsAT	XP_005268811.1:n.1357+297_1357+298delinsAT
XM_005268757.4:c.1276+297_1276+298delinsAT	XP_005268814.1:n.1276+297_1276+298delinsAT
XM_017019098.1:c.1579+297_1579+298delinsAT	XP_016874587.1:n.1579+297_1579+298delinsAT
XM_017019099.1:c.1432+297_1432+298delinsAT	XP_016874588.1:n.1432+297_1432+298delinsAT
XM_017019100.1:c.1423+297_1423+298delinsAT	XP_016874589.1:n.1423+297_1423+298delinsAT
NM_001178074.2:c.1198+297_1198+298delinsAT	NP_001171545.1:n.1198+297_1198+298delinsAT
NM_021150.4:c.1198+297_1198+298delinsAT	NP_066973.2:n.1198+297_1198+298delinsAT
NM_001379345.1:c.1432+297_1432+298delinsAT	NP_001366274.1:n.1432+297_1432+298delinsAT
NM_001379346.1:c.1354+297_1354+298delinsAT	NP_001366275.1:n.1354+297_1354+298delinsAT
NM_001379347.1:c.1276+297_1276+298delinsAT	NP_001366276.1:n.1276+297_1276+298delinsAT
NM_001379348.1:c.1273+297_1273+298delinsAT	NP_001366277.1:n.1273+297_1273+298delinsAT
NM_001379349.1:c.1201+297_1201+298delinsAT	NP_001366278.1:n.1201+297_1201+298delinsAT
NM_001379351.1:c.1198+297_1198+298delinsAT	NP_001366280.1:n.1198+297_1198+298delinsAT