Canonical Allele Identifier: CA2043057233

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66455554C= , CM000674.2:g.66455554C=	GRCh38
NC_000012.11:g.66849334C= , CM000674.1:g.66849334C=	GRCh37
NC_000012.10:g.65135601C=	NCBI36
NG_021400.1:g.228592G=
NG_021400.2:g.618712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696989.1:c.1278G=	ENSP00000513025.1:p.Val426=
ENST00000359742.9:c.1209G= MANE Select	ENSP00000352780.4:p.Val403=
ENST00000359742.8:c.1209G=	ENSP00000352780.4:p.Val403=
ENST00000398016.7:c.1053G=	ENSP00000381098.3:p.Val351=
ENST00000535002.1:c.315G=
ENST00000536215.5:c.874+7370G=	ENSP00000446011.1:n.874+7370G=
ENST00000538164.5:c.653G=
ENST00000538211.5:c.1053G=	ENSP00000446047.1:p.Val351=
ENST00000540433.5:c.885G=	ENSP00000446024.1:p.Val295=
ENST00000540854.5:c.337+60065G=	ENSP00000443006.1:n.337+60065G=
ENST00000543172.5:c.511G=
NM_001178074.1:c.1053G=	NP_001171545.1:p.Val351=
NM_021150.3:c.1053G=	NP_066973.2:p.Val351=
XM_005268754.3:c.1212G=	XP_005268811.1:p.Val404=
XM_005268757.3:c.1131G=	XP_005268814.1:p.Val377=
XM_011538089.1:c.1434G=	XP_011536391.1:p.Val478=
XM_011538090.1:c.1434G=	XP_011536392.1:p.Val478=
XM_011538091.1:c.1278G=	XP_011536393.1:p.Val426=
XM_011538092.1:c.1278G=	XP_011536394.1:p.Val426=
XM_011538093.1:c.1209G=	XP_011536395.1:p.Val403=
XM_011538094.1:c.1041G=	XP_011536396.1:p.Val347=
NM_001366722.1:c.1209G= MANE Select	NP_001353651.1:p.Val403=
NM_001366723.1:c.1128G=	NP_001353652.1:p.Val376=
NM_001366724.1:c.1131G=	NP_001353653.1:p.Val377=
XM_005268754.4:c.1212G=	XP_005268811.1:p.Val404=
XM_005268757.4:c.1131G=	XP_005268814.1:p.Val377=
XM_017019098.1:c.1434G=	XP_016874587.1:p.Val478=
XM_017019099.1:c.1287G=	XP_016874588.1:p.Val429=
XM_017019100.1:c.1278G=	XP_016874589.1:p.Val426=
NM_001178074.2:c.1053G=	NP_001171545.1:p.Val351=
NM_021150.4:c.1053G=	NP_066973.2:p.Val351=
NM_001379345.1:c.1287G=	NP_001366274.1:p.Val429=
NM_001379346.1:c.1209G=	NP_001366275.1:p.Val403=
NM_001379347.1:c.1131G=	NP_001366276.1:p.Val377=
NM_001379348.1:c.1128G=	NP_001366277.1:p.Val376=
NM_001379349.1:c.1056G=	NP_001366278.1:p.Val352=
NM_001379351.1:c.1053G=	NP_001366280.1:p.Val351=