Canonical Allele Identifier: CA2043057153

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455373_66455374delinsTC , CM000674.2:g.66455373_66455374delinsTC	GRCh38
NC_000012.11:g.66849153_66849154delinsTC , CM000674.1:g.66849153_66849154delinsTC	GRCh37
NC_000012.10:g.65135420_65135421delinsTC	NCBI36
NG_021400.1:g.228772_228773delinsGA
NG_021400.2:g.618892_618893delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696989.1:c.1423+35_1423+36delinsGA	ENSP00000513025.1:n.1423+35_1423+36delinsGA
ENST00000359742.9:c.1354+35_1354+36delinsGA MANE Select	ENSP00000352780.4:n.1354+35_1354+36delinsGA
ENST00000359742.8:c.1354+35_1354+36delinsGA	ENSP00000352780.4:n.1354+35_1354+36delinsGA
ENST00000398016.7:c.1198+35_1198+36delinsGA	ENSP00000381098.3:n.1198+35_1198+36delinsGA
ENST00000535002.1:c.460+35_460+36delinsGA
ENST00000536215.5:c.874+7550_874+7551delinsGA	ENSP00000446011.1:n.874+7550_874+7551delinsGA
ENST00000538164.5:c.798+35_798+36delinsGA
ENST00000538211.5:c.1198+35_1198+36delinsGA	ENSP00000446047.1:n.1198+35_1198+36delinsGA
ENST00000540433.5:c.1030+35_1030+36delinsGA	ENSP00000446024.1:n.1030+35_1030+36delinsGA
ENST00000540854.5:c.337+60245_337+60246delinsGA	ENSP00000443006.1:n.337+60245_337+60246delinsGA
ENST00000543172.5:c.656+35_656+36delinsGA
NM_001178074.1:c.1198+35_1198+36delinsGA	NP_001171545.1:n.1198+35_1198+36delinsGA
NM_021150.3:c.1198+35_1198+36delinsGA	NP_066973.2:n.1198+35_1198+36delinsGA
XM_005268754.3:c.1357+35_1357+36delinsGA	XP_005268811.1:n.1357+35_1357+36delinsGA
XM_005268757.3:c.1276+35_1276+36delinsGA	XP_005268814.1:n.1276+35_1276+36delinsGA
XM_011538089.1:c.1579+35_1579+36delinsGA	XP_011536391.1:n.1579+35_1579+36delinsGA
XM_011538090.1:c.1579+35_1579+36delinsGA	XP_011536392.1:n.1579+35_1579+36delinsGA
XM_011538091.1:c.1423+35_1423+36delinsGA	XP_011536393.1:n.1423+35_1423+36delinsGA
XM_011538092.1:c.1423+35_1423+36delinsGA	XP_011536394.1:n.1423+35_1423+36delinsGA
XM_011538093.1:c.1354+35_1354+36delinsGA	XP_011536395.1:n.1354+35_1354+36delinsGA
XM_011538094.1:c.1186+35_1186+36delinsGA	XP_011536396.1:n.1186+35_1186+36delinsGA
NM_001366722.1:c.1354+35_1354+36delinsGA MANE Select	NP_001353651.1:n.1354+35_1354+36delinsGA
NM_001366723.1:c.1273+35_1273+36delinsGA	NP_001353652.1:n.1273+35_1273+36delinsGA
NM_001366724.1:c.1276+35_1276+36delinsGA	NP_001353653.1:n.1276+35_1276+36delinsGA
XM_005268754.4:c.1357+35_1357+36delinsGA	XP_005268811.1:n.1357+35_1357+36delinsGA
XM_005268757.4:c.1276+35_1276+36delinsGA	XP_005268814.1:n.1276+35_1276+36delinsGA
XM_017019098.1:c.1579+35_1579+36delinsGA	XP_016874587.1:n.1579+35_1579+36delinsGA
XM_017019099.1:c.1432+35_1432+36delinsGA	XP_016874588.1:n.1432+35_1432+36delinsGA
XM_017019100.1:c.1423+35_1423+36delinsGA	XP_016874589.1:n.1423+35_1423+36delinsGA
NM_001178074.2:c.1198+35_1198+36delinsGA	NP_001171545.1:n.1198+35_1198+36delinsGA
NM_021150.4:c.1198+35_1198+36delinsGA	NP_066973.2:n.1198+35_1198+36delinsGA
NM_001379345.1:c.1432+35_1432+36delinsGA	NP_001366274.1:n.1432+35_1432+36delinsGA
NM_001379346.1:c.1354+35_1354+36delinsGA	NP_001366275.1:n.1354+35_1354+36delinsGA
NM_001379347.1:c.1276+35_1276+36delinsGA	NP_001366276.1:n.1276+35_1276+36delinsGA
NM_001379348.1:c.1273+35_1273+36delinsGA	NP_001366277.1:n.1273+35_1273+36delinsGA
NM_001379349.1:c.1201+35_1201+36delinsGA	NP_001366278.1:n.1201+35_1201+36delinsGA
NM_001379351.1:c.1198+35_1198+36delinsGA	NP_001366280.1:n.1198+35_1198+36delinsGA