Canonical Allele Identifier: CA2043056749

Gene: GRIP1

Linked Data

• dbSNP Id: rs2057834331

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.66422375_66422391del , CM000674.2:g.66422375_66422391del	GRCh38
NC_000012.11:g.66816155_66816171del , CM000674.1:g.66816155_66816171del	GRCh37
NC_000012.10:g.65102422_65102438del	NCBI36
NG_021400.1:g.261756_261772del
NG_021400.2:g.651876_651892del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696989.1:c.1838-1601_1838-1585del	ENSP00000513025.1:n.1838-1601_1838-1585de...
ENST00000359742.9:c.1769-1601_1769-1585del MANE Select	ENSP00000352780.4:n.1769-1601_1769-1585de...
ENST00000359742.8:c.1769-1601_1769-1585del	ENSP00000352780.4:n.1769-1601_1769-1585de...
ENST00000398016.7:c.1613-1601_1613-1585del	ENSP00000381098.3:n.1613-1601_1613-1585de...
ENST00000536215.5:c.1289-1601_1289-1585del	ENSP00000446011.1:n.1289-1601_1289-1585de...
ENST00000538164.5:c.1213-1601_1213-1585del
ENST00000538211.5:c.1613-1601_1613-1585del	ENSP00000446047.1:n.1613-1601_1613-1585de...
ENST00000540433.5:c.1445-1601_1445-1585del	ENSP00000446024.1:n.1445-1601_1445-1585de...
ENST00000540854.5:c.338-73144_338-73128del	ENSP00000443006.1:n.338-73144_338-73128de...
NM_001178074.1:c.1613-1601_1613-1585del	NP_001171545.1:n.1613-1601_1613-1585del
NM_021150.3:c.1613-1601_1613-1585del	NP_066973.2:n.1613-1601_1613-1585del
XM_005268754.3:c.1772-1601_1772-1585del	XP_005268811.1:n.1772-1601_1772-1585del
XM_005268757.3:c.1691-1601_1691-1585del	XP_005268814.1:n.1691-1601_1691-1585del
XM_011538089.1:c.1994-1601_1994-1585del	XP_011536391.1:n.1994-1601_1994-1585del
XM_011538090.1:c.1994-1601_1994-1585del	XP_011536392.1:n.1994-1601_1994-1585del
XM_011538091.1:c.1838-1601_1838-1585del	XP_011536393.1:n.1838-1601_1838-1585del
XM_011538092.1:c.1838-1601_1838-1585del	XP_011536394.1:n.1838-1601_1838-1585del
XM_011538093.1:c.1769-1601_1769-1585del	XP_011536395.1:n.1769-1601_1769-1585del
XM_011538094.1:c.1601-1601_1601-1585del	XP_011536396.1:n.1601-1601_1601-1585del
NM_001366722.1:c.1769-1601_1769-1585del MANE Select	NP_001353651.1:n.1769-1601_1769-1585del
NM_001366723.1:c.1688-1601_1688-1585del	NP_001353652.1:n.1688-1601_1688-1585del
NM_001366724.1:c.1691-1601_1691-1585del	NP_001353653.1:n.1691-1601_1691-1585del
XM_005268754.4:c.1772-1601_1772-1585del	XP_005268811.1:n.1772-1601_1772-1585del
XM_005268757.4:c.1691-1601_1691-1585del	XP_005268814.1:n.1691-1601_1691-1585del
XM_017019098.1:c.1994-1601_1994-1585del	XP_016874587.1:n.1994-1601_1994-1585del
XM_017019099.1:c.1847-1601_1847-1585del	XP_016874588.1:n.1847-1601_1847-1585del
XM_017019100.1:c.1838-1601_1838-1585del	XP_016874589.1:n.1838-1601_1838-1585del
NM_001178074.2:c.1613-1601_1613-1585del	NP_001171545.1:n.1613-1601_1613-1585del
NM_021150.4:c.1613-1601_1613-1585del	NP_066973.2:n.1613-1601_1613-1585del
NM_001379345.1:c.1847-1601_1847-1585del	NP_001366274.1:n.1847-1601_1847-1585del
NM_001379346.1:c.1769-1601_1769-1585del	NP_001366275.1:n.1769-1601_1769-1585del
NM_001379347.1:c.1691-1601_1691-1585del	NP_001366276.1:n.1691-1601_1691-1585del
NM_001379348.1:c.1688-1601_1688-1585del	NP_001366277.1:n.1688-1601_1688-1585del
NM_001379349.1:c.1616-1601_1616-1585del	NP_001366278.1:n.1616-1601_1616-1585del
NM_001379351.1:c.1613-1601_1613-1585del	NP_001366280.1:n.1613-1601_1613-1585del