Canonical Allele Identifier: CA385626065

Gene: GRIP1

Linked Data

• dbSNP Id: rs764803577
• MyVariant Identifiers: chr12:g.66849267G>T (hg19) ; chr12:g.66455487G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455487G>T , CM000674.2:g.66455487G>T	GRCh38
NC_000012.11:g.66849267G>T , CM000674.1:g.66849267G>T	GRCh37
NC_000012.10:g.65135534G>T	NCBI36
NG_021400.1:g.228659C>A
NG_021400.2:g.618779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696989.1:c.1345C>A	ENSP00000513025.1:p.Pro449Thr
ENST00000359742.9:c.1276C>A MANE Select	ENSP00000352780.4:p.Pro426Thr
ENST00000359742.8:c.1276C>A	ENSP00000352780.4:p.Pro426Thr
ENST00000398016.7:c.1120C>A	ENSP00000381098.3:p.Pro374Thr
ENST00000535002.1:c.382C>A
ENST00000536215.5:c.874+7437C>A	ENSP00000446011.1:n.874+7437C>A
ENST00000538164.5:c.720C>A
ENST00000538211.5:c.1120C>A	ENSP00000446047.1:p.Pro374Thr
ENST00000540433.5:c.952C>A	ENSP00000446024.1:p.Pro318Thr
ENST00000540854.5:c.337+60132C>A	ENSP00000443006.1:n.337+60132C>A
ENST00000543172.5:c.578C>A
NM_001178074.1:c.1120C>A	NP_001171545.1:p.Pro374Thr
NM_021150.3:c.1120C>A	NP_066973.2:p.Pro374Thr
XM_005268754.3:c.1279C>A	XP_005268811.1:p.Pro427Thr
XM_005268757.3:c.1198C>A	XP_005268814.1:p.Pro400Thr
XM_011538089.1:c.1501C>A	XP_011536391.1:p.Pro501Thr
XM_011538090.1:c.1501C>A	XP_011536392.1:p.Pro501Thr
XM_011538091.1:c.1345C>A	XP_011536393.1:p.Pro449Thr
XM_011538092.1:c.1345C>A	XP_011536394.1:p.Pro449Thr
XM_011538093.1:c.1276C>A	XP_011536395.1:p.Pro426Thr
XM_011538094.1:c.1108C>A	XP_011536396.1:p.Pro370Thr
NM_001366722.1:c.1276C>A MANE Select	NP_001353651.1:p.Pro426Thr
NM_001366723.1:c.1195C>A	NP_001353652.1:p.Pro399Thr
NM_001366724.1:c.1198C>A	NP_001353653.1:p.Pro400Thr
XM_005268754.4:c.1279C>A	XP_005268811.1:p.Pro427Thr
XM_005268757.4:c.1198C>A	XP_005268814.1:p.Pro400Thr
XM_017019098.1:c.1501C>A	XP_016874587.1:p.Pro501Thr
XM_017019099.1:c.1354C>A	XP_016874588.1:p.Pro452Thr
XM_017019100.1:c.1345C>A	XP_016874589.1:p.Pro449Thr
NM_001178074.2:c.1120C>A	NP_001171545.1:p.Pro374Thr
NM_021150.4:c.1120C>A	NP_066973.2:p.Pro374Thr
NM_001379345.1:c.1354C>A	NP_001366274.1:p.Pro452Thr
NM_001379346.1:c.1276C>A	NP_001366275.1:p.Pro426Thr
NM_001379347.1:c.1198C>A	NP_001366276.1:p.Pro400Thr
NM_001379348.1:c.1195C>A	NP_001366277.1:p.Pro399Thr
NM_001379349.1:c.1123C>A	NP_001366278.1:p.Pro375Thr
NM_001379351.1:c.1120C>A	NP_001366280.1:p.Pro374Thr