Canonical Allele Identifier: CA6674423

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455494C>T , CM000674.2:g.66455494C>T	GRCh38
NC_000012.11:g.66849274C>T , CM000674.1:g.66849274C>T	GRCh37
NC_000012.10:g.65135541C>T	NCBI36
NG_021400.1:g.228652G>A
NG_021400.2:g.618772G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001366722.1:c.1269G>A MANE Select	NP_001353651.1:p.Gly423=
ENST00000359742.9:c.1269G>A MANE Select	ENSP00000352780.4:p.Gly423=
NM_001178074.1:c.1113G>A	NP_001171545.1:p.Gly371=
NM_001178074.2:c.1113G>A	NP_001171545.1:p.Gly371=
NM_001366723.1:c.1188G>A	NP_001353652.1:p.Gly396=
NM_001366724.1:c.1191G>A	NP_001353653.1:p.Gly397=
NM_001379345.1:c.1347G>A	NP_001366274.1:p.Gly449=
NM_001379346.1:c.1269G>A	NP_001366275.1:p.Gly423=
NM_001379347.1:c.1191G>A	NP_001366276.1:p.Gly397=
NM_001379348.1:c.1188G>A	NP_001366277.1:p.Gly396=
NM_001379349.1:c.1116G>A	NP_001366278.1:p.Gly372=
NM_001379351.1:c.1113G>A	NP_001366280.1:p.Gly371=
NM_021150.3:c.1113G>A	NP_066973.2:p.Gly371=
NM_021150.4:c.1113G>A	NP_066973.2:p.Gly371=
ENST00000359742.8:c.1269G>A	ENSP00000352780.4:p.Gly423=
ENST00000398016.7:c.1113G>A	ENSP00000381098.3:p.Gly371=
ENST00000535002.1:c.375G>A
ENST00000536215.5:c.874+7430G>A	ENSP00000446011.1:n.874+7430G>A
ENST00000538164.5:c.713G>A
ENST00000538211.5:c.1113G>A	ENSP00000446047.1:p.Gly371=
ENST00000540433.5:c.945G>A	ENSP00000446024.1:p.Gly315=
ENST00000540854.5:c.337+60125G>A	ENSP00000443006.1:n.337+60125G>A
ENST00000543172.5:c.571G>A
ENST00000696989.1:c.1338G>A	ENSP00000513025.1:p.Gly446=
XM_005268754.3:c.1272G>A	XP_005268811.1:p.Gly424=
XM_005268754.4:c.1272G>A	XP_005268811.1:p.Gly424=
XM_005268757.3:c.1191G>A	XP_005268814.1:p.Gly397=
XM_005268757.4:c.1191G>A	XP_005268814.1:p.Gly397=
XM_011538089.1:c.1494G>A	XP_011536391.1:p.Gly498=
XM_011538090.1:c.1494G>A	XP_011536392.1:p.Gly498=
XM_011538091.1:c.1338G>A	XP_011536393.1:p.Gly446=
XM_011538092.1:c.1338G>A	XP_011536394.1:p.Gly446=
XM_011538093.1:c.1269G>A	XP_011536395.1:p.Gly423=
XM_011538094.1:c.1101G>A	XP_011536396.1:p.Gly367=
XM_017019098.1:c.1494G>A	XP_016874587.1:p.Gly498=
XM_017019099.1:c.1347G>A	XP_016874588.1:p.Gly449=
XM_017019100.1:c.1338G>A	XP_016874589.1:p.Gly446=