Canonical Allele Identifier: CA2619715982

Gene: GRIP1

Linked Data

• gnomAD v4: 12-66455269-ACAGAGCTGTTAGCTGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455273_66455289del , CM000674.2:g.66455273_66455289del	GRCh38
NC_000012.11:g.66849053_66849069del , CM000674.1:g.66849053_66849069del	GRCh37
NC_000012.10:g.65135320_65135336del	NCBI36
NG_021400.1:g.228860_228876del
NG_021400.2:g.618980_618996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696989.1:c.1423+123_1423+139del	ENSP00000513025.1:n.1423+123_1423+139del
ENST00000359742.9:c.1354+123_1354+139del MANE Select	ENSP00000352780.4:n.1354+123_1354+139del
ENST00000359742.8:c.1354+123_1354+139del	ENSP00000352780.4:n.1354+123_1354+139del
ENST00000398016.7:c.1198+123_1198+139del	ENSP00000381098.3:n.1198+123_1198+139del
ENST00000535002.1:c.460+123_460+139del
ENST00000536215.5:c.874+7638_874+7654del	ENSP00000446011.1:n.874+7638_874+7654del
ENST00000538164.5:c.798+123_798+139del
ENST00000538211.5:c.1198+123_1198+139del	ENSP00000446047.1:n.1198+123_1198+139del
ENST00000540433.5:c.1030+123_1030+139del	ENSP00000446024.1:n.1030+123_1030+139del
ENST00000540854.5:c.337+60333_337+60349del	ENSP00000443006.1:n.337+60333_337+60349del
ENST00000543172.5:c.656+123_656+139del
NM_001178074.1:c.1198+123_1198+139del	NP_001171545.1:n.1198+123_1198+139del
NM_021150.3:c.1198+123_1198+139del	NP_066973.2:n.1198+123_1198+139del
XM_005268754.3:c.1357+123_1357+139del	XP_005268811.1:n.1357+123_1357+139del
XM_005268757.3:c.1276+123_1276+139del	XP_005268814.1:n.1276+123_1276+139del
XM_011538089.1:c.1579+123_1579+139del	XP_011536391.1:n.1579+123_1579+139del
XM_011538090.1:c.1579+123_1579+139del	XP_011536392.1:n.1579+123_1579+139del
XM_011538091.1:c.1423+123_1423+139del	XP_011536393.1:n.1423+123_1423+139del
XM_011538092.1:c.1423+123_1423+139del	XP_011536394.1:n.1423+123_1423+139del
XM_011538093.1:c.1354+123_1354+139del	XP_011536395.1:n.1354+123_1354+139del
XM_011538094.1:c.1186+123_1186+139del	XP_011536396.1:n.1186+123_1186+139del
NM_001366722.1:c.1354+123_1354+139del MANE Select	NP_001353651.1:n.1354+123_1354+139del
NM_001366723.1:c.1273+123_1273+139del	NP_001353652.1:n.1273+123_1273+139del
NM_001366724.1:c.1276+123_1276+139del	NP_001353653.1:n.1276+123_1276+139del
XM_005268754.4:c.1357+123_1357+139del	XP_005268811.1:n.1357+123_1357+139del
XM_005268757.4:c.1276+123_1276+139del	XP_005268814.1:n.1276+123_1276+139del
XM_017019098.1:c.1579+123_1579+139del	XP_016874587.1:n.1579+123_1579+139del
XM_017019099.1:c.1432+123_1432+139del	XP_016874588.1:n.1432+123_1432+139del
XM_017019100.1:c.1423+123_1423+139del	XP_016874589.1:n.1423+123_1423+139del
NM_001178074.2:c.1198+123_1198+139del	NP_001171545.1:n.1198+123_1198+139del
NM_021150.4:c.1198+123_1198+139del	NP_066973.2:n.1198+123_1198+139del
NM_001379345.1:c.1432+123_1432+139del	NP_001366274.1:n.1432+123_1432+139del
NM_001379346.1:c.1354+123_1354+139del	NP_001366275.1:n.1354+123_1354+139del
NM_001379347.1:c.1276+123_1276+139del	NP_001366276.1:n.1276+123_1276+139del
NM_001379348.1:c.1273+123_1273+139del	NP_001366277.1:n.1273+123_1273+139del
NM_001379349.1:c.1201+123_1201+139del	NP_001366278.1:n.1201+123_1201+139del
NM_001379351.1:c.1198+123_1198+139del	NP_001366280.1:n.1198+123_1198+139del