Canonical Allele Identifier: CA2043056686

Gene: GRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66422305_66422306delinsGC , CM000674.2:g.66422305_66422306delinsGC	GRCh38
NC_000012.11:g.66816085_66816086delinsGC , CM000674.1:g.66816085_66816086delinsGC	GRCh37
NC_000012.10:g.65102352_65102353delinsGC	NCBI36
NG_021400.1:g.261840_261841delinsGC
NG_021400.2:g.651960_651961delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696989.1:c.1838-1517_1838-1516delinsGC	ENSP00000513025.1:n.1838-1517_1838-1516de...
ENST00000359742.9:c.1769-1517_1769-1516delinsGC MANE Select	ENSP00000352780.4:n.1769-1517_1769-1516de...
ENST00000359742.8:c.1769-1517_1769-1516delinsGC	ENSP00000352780.4:n.1769-1517_1769-1516de...
ENST00000398016.7:c.1613-1517_1613-1516delinsGC	ENSP00000381098.3:n.1613-1517_1613-1516de...
ENST00000536215.5:c.1289-1517_1289-1516delinsGC	ENSP00000446011.1:n.1289-1517_1289-1516de...
ENST00000538164.5:c.1213-1517_1213-1516delinsGC
ENST00000538211.5:c.1613-1517_1613-1516delinsGC	ENSP00000446047.1:n.1613-1517_1613-1516de...
ENST00000540433.5:c.1445-1517_1445-1516delinsGC	ENSP00000446024.1:n.1445-1517_1445-1516de...
ENST00000540854.5:c.338-73060_338-73059delinsGC	ENSP00000443006.1:n.338-73060_338-73059de...
NM_001178074.1:c.1613-1517_1613-1516delinsGC	NP_001171545.1:n.1613-1517_1613-1516delin...
NM_021150.3:c.1613-1517_1613-1516delinsGC	NP_066973.2:n.1613-1517_1613-1516delinsGC...
XM_005268754.3:c.1772-1517_1772-1516delinsGC	XP_005268811.1:n.1772-1517_1772-1516delin...
XM_005268757.3:c.1691-1517_1691-1516delinsGC	XP_005268814.1:n.1691-1517_1691-1516delin...
XM_011538089.1:c.1994-1517_1994-1516delinsGC	XP_011536391.1:n.1994-1517_1994-1516delin...
XM_011538090.1:c.1994-1517_1994-1516delinsGC	XP_011536392.1:n.1994-1517_1994-1516delin...
XM_011538091.1:c.1838-1517_1838-1516delinsGC	XP_011536393.1:n.1838-1517_1838-1516delin...
XM_011538092.1:c.1838-1517_1838-1516delinsGC	XP_011536394.1:n.1838-1517_1838-1516delin...
XM_011538093.1:c.1769-1517_1769-1516delinsGC	XP_011536395.1:n.1769-1517_1769-1516delin...
XM_011538094.1:c.1601-1517_1601-1516delinsGC	XP_011536396.1:n.1601-1517_1601-1516delin...
NM_001366722.1:c.1769-1517_1769-1516delinsGC MANE Select	NP_001353651.1:n.1769-1517_1769-1516delin...
NM_001366723.1:c.1688-1517_1688-1516delinsGC	NP_001353652.1:n.1688-1517_1688-1516delin...
NM_001366724.1:c.1691-1517_1691-1516delinsGC	NP_001353653.1:n.1691-1517_1691-1516delin...
XM_005268754.4:c.1772-1517_1772-1516delinsGC	XP_005268811.1:n.1772-1517_1772-1516delin...
XM_005268757.4:c.1691-1517_1691-1516delinsGC	XP_005268814.1:n.1691-1517_1691-1516delin...
XM_017019098.1:c.1994-1517_1994-1516delinsGC	XP_016874587.1:n.1994-1517_1994-1516delin...
XM_017019099.1:c.1847-1517_1847-1516delinsGC	XP_016874588.1:n.1847-1517_1847-1516delin...
XM_017019100.1:c.1838-1517_1838-1516delinsGC	XP_016874589.1:n.1838-1517_1838-1516delin...
NM_001178074.2:c.1613-1517_1613-1516delinsGC	NP_001171545.1:n.1613-1517_1613-1516delin...
NM_021150.4:c.1613-1517_1613-1516delinsGC	NP_066973.2:n.1613-1517_1613-1516delinsGC...
NM_001379345.1:c.1847-1517_1847-1516delinsGC	NP_001366274.1:n.1847-1517_1847-1516delin...
NM_001379346.1:c.1769-1517_1769-1516delinsGC	NP_001366275.1:n.1769-1517_1769-1516delin...
NM_001379347.1:c.1691-1517_1691-1516delinsGC	NP_001366276.1:n.1691-1517_1691-1516delin...
NM_001379348.1:c.1688-1517_1688-1516delinsGC	NP_001366277.1:n.1688-1517_1688-1516delin...
NM_001379349.1:c.1616-1517_1616-1516delinsGC	NP_001366278.1:n.1616-1517_1616-1516delin...
NM_001379351.1:c.1613-1517_1613-1516delinsGC	NP_001366280.1:n.1613-1517_1613-1516delin...