Canonical Allele Identifier: CA1290527746
Gene: RAB3GAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135135571_135135574delinsATTG , CM000664.2:g.135135571_135135574delinsATTG GRCh38
NC_000002.11:g.135893141_135893144delinsATTG , CM000664.1:g.135893141_135893144delinsATTG GRCh37
NC_000002.10:g.135609611_135609614delinsATTG NCBI36
NG_016972.1:g.88307_88310delinsATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.1562_1565delinsATTG ENSP00000444306.2:p.Asn521=
ENST00000685967.1:c.*1019_*1022delinsATTG ENSP00000508423.1:n.*1019_*1022delinsATTG
ENST00000686114.1:n.1908_1911delinsATTG
ENST00000687199.1:c.*1630_*1633delinsATTG ENSP00000510319.1:n.*1630_*1633delinsATTG
ENST00000688088.1:n.1581_1584delinsATTG
ENST00000688182.1:c.151-32122_151-32119delinsATTG ENSP00000509324.1:n.151-32122_151-32119delinsATTG
ENST00000689880.1:n.1581_1584delinsATTG
ENST00000690208.1:c.*1240_*1243delinsATTG ENSP00000510746.1:n.*1240_*1243delinsATTG
ENST00000690785.1:n.1581_1584delinsATTG
ENST00000691339.1:c.*1185_*1188delinsATTG ENSP00000509953.1:n.*1185_*1188delinsATTG
ENST00000691478.1:c.*1661_*1664delinsATTG ENSP00000509081.1:n.*1661_*1664delinsATTG
ENST00000693554.1:c.1562_1565delinsATTG ENSP00000509030.1:p.Asn521=
ENST00000264158.13:c.1562_1565delinsATTG MANE Select ENSP00000264158.8:p.Asn521=
ENST00000264158.12:c.1562_1565delinsATTG ENSP00000264158.7:p.Asn521=
ENST00000442034.5:c.1562_1565delinsATTG ENSP00000411418.1:p.Asn521=
ENST00000487003.5:n.1631_1634delinsATTG
ENST00000539493.2:c.1430_1433delinsATTG ENSP00000444306.1:p.Asn477=
NM_001172435.1:c.1562_1565delinsATTG NP_001165906.1:p.Asn521=
NM_012233.2:c.1562_1565delinsATTG NP_036365.1:p.Asn521=
XM_011510822.1:c.1562_1565delinsATTG XP_011509124.1:p.Asn521=
XM_011510823.1:c.1562_1565delinsATTG XP_011509125.1:p.Asn521=
XM_011510824.1:c.1562_1565delinsATTG XP_011509126.1:p.Asn521=
XM_011510825.1:c.1562_1565delinsATTG XP_011509127.1:p.Asn521=
XM_011510823.3:c.1562_1565delinsATTG XP_011509125.1:p.Asn521=
XM_011510825.3:c.1562_1565delinsATTG XP_011509127.1:p.Asn521=
XR_001738674.2:n.1589_1592delinsATTG
NM_001172435.2:c.1562_1565delinsATTG NP_001165906.1:p.Asn521=
NM_012233.3:c.1562_1565delinsATTG MANE Select NP_036365.1:p.Asn521=