Canonical Allele Identifier: CA6674374

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66445435C>T , CM000674.2:g.66445435C>T	GRCh38
NC_000012.11:g.66839215C>T , CM000674.1:g.66839215C>T	GRCh37
NC_000012.10:g.65125482C>T	NCBI36
NG_021400.1:g.238711G>A
NG_021400.2:g.628831G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001366722.1:c.1428G>A MANE Select	NP_001353651.1:p.Thr476=
ENST00000359742.9:c.1428G>A MANE Select	ENSP00000352780.4:p.Thr476=
NM_001178074.1:c.1272G>A	NP_001171545.1:p.Thr424=
NM_001178074.2:c.1272G>A	NP_001171545.1:p.Thr424=
NM_001366723.1:c.1347G>A	NP_001353652.1:p.Thr449=
NM_001366724.1:c.1350G>A	NP_001353653.1:p.Thr450=
NM_001379345.1:c.1506G>A	NP_001366274.1:p.Thr502=
NM_001379346.1:c.1428G>A	NP_001366275.1:p.Thr476=
NM_001379347.1:c.1350G>A	NP_001366276.1:p.Thr450=
NM_001379348.1:c.1347G>A	NP_001366277.1:p.Thr449=
NM_001379349.1:c.1275G>A	NP_001366278.1:p.Thr425=
NM_001379351.1:c.1272G>A	NP_001366280.1:p.Thr424=
NM_021150.3:c.1272G>A	NP_066973.2:p.Thr424=
NM_021150.4:c.1272G>A	NP_066973.2:p.Thr424=
ENST00000359742.8:c.1428G>A	ENSP00000352780.4:p.Thr476=
ENST00000398016.7:c.1272G>A	ENSP00000381098.3:p.Thr424=
ENST00000535002.1:c.534G>A
ENST00000536215.5:c.948G>A	ENSP00000446011.1:p.Thr316=
ENST00000538164.5:c.872G>A
ENST00000538211.5:c.1272G>A	ENSP00000446047.1:p.Thr424=
ENST00000540433.5:c.1104G>A	ENSP00000446024.1:p.Thr368=
ENST00000540854.5:c.337+70184G>A	ENSP00000443006.1:n.337+70184G>A
ENST00000543172.5:c.730G>A
ENST00000696989.1:c.1497G>A	ENSP00000513025.1:p.Thr499=
XM_005268754.3:c.1431G>A	XP_005268811.1:p.Thr477=
XM_005268754.4:c.1431G>A	XP_005268811.1:p.Thr477=
XM_005268757.3:c.1350G>A	XP_005268814.1:p.Thr450=
XM_005268757.4:c.1350G>A	XP_005268814.1:p.Thr450=
XM_011538089.1:c.1653G>A	XP_011536391.1:p.Thr551=
XM_011538090.1:c.1653G>A	XP_011536392.1:p.Thr551=
XM_011538091.1:c.1497G>A	XP_011536393.1:p.Thr499=
XM_011538092.1:c.1497G>A	XP_011536394.1:p.Thr499=
XM_011538093.1:c.1428G>A	XP_011536395.1:p.Thr476=
XM_011538094.1:c.1260G>A	XP_011536396.1:p.Thr420=
XM_017019098.1:c.1653G>A	XP_016874587.1:p.Thr551=
XM_017019099.1:c.1506G>A	XP_016874588.1:p.Thr502=
XM_017019100.1:c.1497G>A	XP_016874589.1:p.Thr499=