Canonical Allele Identifier: CA1290527763
Gene: RAB3GAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135135608_135135610delinsGAA , CM000664.2:g.135135608_135135610delinsGAA GRCh38
NC_000002.11:g.135893178_135893180delinsGAA , CM000664.1:g.135893178_135893180delinsGAA GRCh37
NC_000002.10:g.135609648_135609650delinsGAA NCBI36
NG_016972.1:g.88344_88346delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.1599_1601delinsGAA ENSP00000444306.2:p.Gly533=
ENST00000685967.1:c.*1056_*1058delinsGAA ENSP00000508423.1:n.*1056_*1058delinsGAA
ENST00000686114.1:n.1945_1947delinsGAA
ENST00000687199.1:c.*1667_*1669delinsGAA ENSP00000510319.1:n.*1667_*1669delinsGAA
ENST00000688088.1:n.1618_1620delinsGAA
ENST00000688182.1:c.151-32085_151-32083delinsGAA ENSP00000509324.1:n.151-32085_151-32083delinsGAA
ENST00000689880.1:n.1618_1620delinsGAA
ENST00000690208.1:c.*1277_*1279delinsGAA ENSP00000510746.1:n.*1277_*1279delinsGAA
ENST00000690785.1:n.1618_1620delinsGAA
ENST00000691339.1:c.*1222_*1224delinsGAA ENSP00000509953.1:n.*1222_*1224delinsGAA
ENST00000691478.1:c.*1698_*1700delinsGAA ENSP00000509081.1:n.*1698_*1700delinsGAA
ENST00000693554.1:c.1599_1601delinsGAA ENSP00000509030.1:p.Gly533=
ENST00000264158.13:c.1599_1601delinsGAA MANE Select ENSP00000264158.8:p.Gly533=
ENST00000264158.12:c.1599_1601delinsGAA ENSP00000264158.7:p.Gly533=
ENST00000442034.5:c.1599_1601delinsGAA ENSP00000411418.1:p.Gly533=
ENST00000487003.5:n.1668_1670delinsGAA
ENST00000539493.2:c.1467_1469delinsGAA ENSP00000444306.1:p.Gly489=
NM_001172435.1:c.1599_1601delinsGAA NP_001165906.1:p.Gly533=
NM_012233.2:c.1599_1601delinsGAA NP_036365.1:p.Gly533=
XM_011510822.1:c.1599_1601delinsGAA XP_011509124.1:p.Gly533=
XM_011510823.1:c.1599_1601delinsGAA XP_011509125.1:p.Gly533=
XM_011510824.1:c.1599_1601delinsGAA XP_011509126.1:p.Gly533=
XM_011510825.1:c.1599_1601delinsGAA XP_011509127.1:p.Gly533=
XM_011510823.3:c.1599_1601delinsGAA XP_011509125.1:p.Gly533=
XM_011510825.3:c.1599_1601delinsGAA XP_011509127.1:p.Gly533=
XR_001738674.2:n.1626_1628delinsGAA
NM_001172435.2:c.1599_1601delinsGAA NP_001165906.1:p.Gly533=
NM_012233.3:c.1599_1601delinsGAA MANE Select NP_036365.1:p.Gly533=