Canonical Allele Identifier: CA480572929

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66371892A>G , CM000674.2:g.66371892A>G	GRCh38
NC_000012.11:g.66765672A>G , CM000674.1:g.66765672A>G	GRCh37
NC_000012.10:g.65051939A>G	NCBI36
NG_021400.1:g.312254T>C
NG_021400.2:g.702374T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001366722.1:c.2814T>C MANE Select	NP_001353651.1:p.Asn938=
ENST00000359742.9:c.2814T>C MANE Select	ENSP00000352780.4:p.Asn938=
NM_001178074.1:c.2613T>C	NP_001171545.1:p.Asn871=
NM_001178074.2:c.2613T>C	NP_001171545.1:p.Asn871=
NM_001366723.1:c.2733T>C	NP_001353652.1:p.Asn911=
NM_001366724.1:c.2736T>C	NP_001353653.1:p.Asn912=
NM_001379345.1:c.2892T>C	NP_001366274.1:p.Asn964=
NM_001379346.1:c.2769T>C	NP_001366275.1:p.Asn923=
NM_001379347.1:c.2691T>C	NP_001366276.1:p.Asn897=
NM_001379348.1:c.2688T>C	NP_001366277.1:p.Asn896=
NM_001379349.1:c.2661T>C	NP_001366278.1:p.Asn887=
NM_001379351.1:c.2613T>C	NP_001366280.1:p.Asn871=
NM_021150.3:c.2658T>C	NP_066973.2:p.Asn886=
NM_021150.4:c.2658T>C	NP_066973.2:p.Asn886=
ENST00000359742.8:c.2814T>C	ENSP00000352780.4:p.Asn938=
ENST00000398016.7:c.2658T>C	ENSP00000381098.3:p.Asn886=
ENST00000535323.1:n.450T>C
ENST00000536215.5:c.2289T>C	ENSP00000446011.1:p.Asn763=
ENST00000538164.5:c.2213T>C
ENST00000538211.5:c.2613T>C	ENSP00000446047.1:p.Asn871=
ENST00000540433.5:c.2490T>C	ENSP00000446024.1:p.Asn830=
ENST00000540854.5:c.338-22646T>C	ENSP00000443006.1:n.338-22646T>C
ENST00000541299.1:n.530T>C
ENST00000696989.1:c.2838T>C	ENSP00000513025.1:p.Asn946=
XM_005268754.3:c.2817T>C	XP_005268811.1:p.Asn939=
XM_005268754.4:c.2817T>C	XP_005268811.1:p.Asn939=
XM_005268757.3:c.2736T>C	XP_005268814.1:p.Asn912=
XM_005268757.4:c.2736T>C	XP_005268814.1:p.Asn912=
XM_011538089.1:c.3039T>C	XP_011536391.1:p.Asn1013=
XM_011538090.1:c.2994T>C	XP_011536392.1:p.Asn998=
XM_011538091.1:c.2883T>C	XP_011536393.1:p.Asn961=
XM_011538092.1:c.2838T>C	XP_011536394.1:p.Asn946=
XM_011538093.1:c.2814T>C	XP_011536395.1:p.Asn938=
XM_011538094.1:c.2646T>C	XP_011536396.1:p.Asn882=
XM_017019098.1:c.2994T>C	XP_016874587.1:p.Asn998=
XM_017019099.1:c.2892T>C	XP_016874588.1:p.Asn964=
XM_017019100.1:c.2838T>C	XP_016874589.1:p.Asn946=