Canonical Allele Identifier: CA385680496

Gene: GRIP1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66678882C>G , CM000674.2:g.66678882C>G	GRCh38
NC_000012.11:g.67072662C>G , CM000674.1:g.67072662C>G	GRCh37
NC_000012.10:g.65358929C>G	NCBI36
NG_021400.1:g.5264G>C
NG_021400.2:g.395384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359742.9:c.23G>C MANE Select	ENSP00000352780.4:p.Cys8Ser
ENST00000643019.1:c.59-81955G>C	ENSP00000495444.1:n.59-81955G>C
ENST00000359742.8:c.23G>C	ENSP00000352780.4:p.Cys8Ser
ENST00000398016.7:c.23G>C	ENSP00000381098.3:p.Cys8Ser
ENST00000538211.5:c.23G>C	ENSP00000446047.1:p.Cys8Ser
ENST00000538373.1:c.-419-48546G>C	ENSP00000446067.1:n.-419-48546G>C
ENST00000539540.5:c.-113-81955G>C	ENSP00000443392.1:n.-113-81955G>C
ENST00000540433.5:c.-33+125050G>C	ENSP00000446024.1:n.-33+125050G>C
ENST00000541947.1:c.134-81955G>C	ENSP00000438921.1:n.134-81955G>C
ENST00000545666.5:c.23G>C	ENSP00000439124.2:p.Cys8Ser
NM_001178074.1:c.23G>C	NP_001171545.1:p.Cys8Ser
NM_021150.3:c.23G>C	NP_066973.2:p.Cys8Ser
XM_005268754.3:c.59-81955G>C	XP_005268811.1:n.59-81955G>C
XM_005268757.3:c.59-136932G>C	XP_005268814.1:n.59-136932G>C
XM_011538093.1:c.23G>C	XP_011536395.1:p.Cys8Ser
NM_001366722.1:c.23G>C MANE Select	NP_001353651.1:p.Cys8Ser
NM_001366723.1:c.134-81955G>C	NP_001353652.1:n.134-81955G>C
NM_001366724.1:c.134-81955G>C	NP_001353653.1:n.134-81955G>C
XM_005268754.4:c.59-81955G>C	XP_005268811.1:n.59-81955G>C
XM_005268757.4:c.59-136932G>C	XP_005268814.1:n.59-136932G>C
XM_017019099.1:c.134-81955G>C	XP_016874588.1:n.134-81955G>C
NM_001178074.2:c.23G>C	NP_001171545.1:p.Cys8Ser
NM_021150.4:c.23G>C	NP_066973.2:p.Cys8Ser
NM_001379345.1:c.134-81955G>C	NP_001366274.1:n.134-81955G>C
NM_001379346.1:c.23G>C	NP_001366275.1:p.Cys8Ser
NM_001379347.1:c.134-81955G>C	NP_001366276.1:n.134-81955G>C
NM_001379348.1:c.134-81955G>C	NP_001366277.1:n.134-81955G>C
NM_001379349.1:c.59-81955G>C	NP_001366278.1:n.59-81955G>C
NM_001379351.1:c.59-81955G>C	NP_001366280.1:n.59-81955G>C