Canonical Allele Identifier: CA1290527754
Gene: RAB3GAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135135596_135135597delinsAC , CM000664.2:g.135135596_135135597delinsAC GRCh38
NC_000002.11:g.135893166_135893167delinsAC , CM000664.1:g.135893166_135893167delinsAC GRCh37
NC_000002.10:g.135609636_135609637delinsAC NCBI36
NG_016972.1:g.88332_88333delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.1587_1588delinsAC ENSP00000444306.2:p.Ala529=
ENST00000685967.1:c.*1044_*1045delinsAC ENSP00000508423.1:n.*1044_*1045delinsAC
ENST00000686114.1:n.1933_1934delinsAC
ENST00000687199.1:c.*1655_*1656delinsAC ENSP00000510319.1:n.*1655_*1656delinsAC
ENST00000688088.1:n.1606_1607delinsAC
ENST00000688182.1:c.151-32097_151-32096delinsAC ENSP00000509324.1:n.151-32097_151-32096delinsAC
ENST00000689880.1:n.1606_1607delinsAC
ENST00000690208.1:c.*1265_*1266delinsAC ENSP00000510746.1:n.*1265_*1266delinsAC
ENST00000690785.1:n.1606_1607delinsAC
ENST00000691339.1:c.*1210_*1211delinsAC ENSP00000509953.1:n.*1210_*1211delinsAC
ENST00000691478.1:c.*1686_*1687delinsAC ENSP00000509081.1:n.*1686_*1687delinsAC
ENST00000693554.1:c.1587_1588delinsAC ENSP00000509030.1:p.Ala529=
ENST00000264158.13:c.1587_1588delinsAC MANE Select ENSP00000264158.8:p.Ala529=
ENST00000264158.12:c.1587_1588delinsAC ENSP00000264158.7:p.Ala529=
ENST00000442034.5:c.1587_1588delinsAC ENSP00000411418.1:p.Ala529=
ENST00000487003.5:n.1656_1657delinsAC
ENST00000539493.2:c.1455_1456delinsAC ENSP00000444306.1:p.Ala485=
NM_001172435.1:c.1587_1588delinsAC NP_001165906.1:p.Ala529=
NM_012233.2:c.1587_1588delinsAC NP_036365.1:p.Ala529=
XM_011510822.1:c.1587_1588delinsAC XP_011509124.1:p.Ala529=
XM_011510823.1:c.1587_1588delinsAC XP_011509125.1:p.Ala529=
XM_011510824.1:c.1587_1588delinsAC XP_011509126.1:p.Ala529=
XM_011510825.1:c.1587_1588delinsAC XP_011509127.1:p.Ala529=
XM_011510823.3:c.1587_1588delinsAC XP_011509125.1:p.Ala529=
XM_011510825.3:c.1587_1588delinsAC XP_011509127.1:p.Ala529=
XR_001738674.2:n.1614_1615delinsAC
NM_001172435.2:c.1587_1588delinsAC NP_001165906.1:p.Ala529=
NM_012233.3:c.1587_1588delinsAC MANE Select NP_036365.1:p.Ala529=