Canonical Allele Identifier: CA1290527735
Gene: RAB3GAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135135551_135135556delinsCTCTTT , CM000664.2:g.135135551_135135556delinsCTCTTT GRCh38
NC_000002.11:g.135893121_135893126delinsCTCTTT , CM000664.1:g.135893121_135893126delinsCTCTTT GRCh37
NC_000002.10:g.135609591_135609596delinsCTCTTT NCBI36
NG_016972.1:g.88287_88292delinsCTCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.1555-13_1555-8delinsCTCTTT ENSP00000444306.2:n.1555-13_1555-8delinsCTCTTT
ENST00000685967.1:c.*1012-13_*1012-8delinsCTCTTT ENSP00000508423.1:n.*1012-13_*1012-8delinsCTCTTT
ENST00000686114.1:n.1901-13_1901-8delinsCTCTTT
ENST00000687199.1:c.*1623-13_*1623-8delinsCTCTTT ENSP00000510319.1:n.*1623-13_*1623-8delinsCTCTTT
ENST00000688088.1:n.1574-13_1574-8delinsCTCTTT
ENST00000688182.1:c.151-32142_151-32137delinsCTCTTT ENSP00000509324.1:n.151-32142_151-32137delinsCTCTTT
ENST00000689880.1:n.1574-13_1574-8delinsCTCTTT
ENST00000690208.1:c.*1233-13_*1233-8delinsCTCTTT ENSP00000510746.1:n.*1233-13_*1233-8delinsCTCTTT
ENST00000690785.1:n.1574-13_1574-8delinsCTCTTT
ENST00000691339.1:c.*1178-13_*1178-8delinsCTCTTT ENSP00000509953.1:n.*1178-13_*1178-8delinsCTCTTT
ENST00000691478.1:c.*1654-13_*1654-8delinsCTCTTT ENSP00000509081.1:n.*1654-13_*1654-8delinsCTCTTT
ENST00000693554.1:c.1555-13_1555-8delinsCTCTTT ENSP00000509030.1:n.1555-13_1555-8delinsCTCTTT
ENST00000264158.13:c.1555-13_1555-8delinsCTCTTT MANE Select ENSP00000264158.8:n.1555-13_1555-8delinsCTCTTT
ENST00000264158.12:c.1555-13_1555-8delinsCTCTTT ENSP00000264158.7:n.1555-13_1555-8delinsCTCTTT
ENST00000442034.5:c.1555-13_1555-8delinsCTCTTT ENSP00000411418.1:n.1555-13_1555-8delinsCTCTTT
ENST00000487003.5:n.1624-13_1624-8delinsCTCTTT
ENST00000539493.2:c.1423-13_1423-8delinsCTCTTT ENSP00000444306.1:n.1423-13_1423-8delinsCTCTTT
NM_001172435.1:c.1555-13_1555-8delinsCTCTTT NP_001165906.1:n.1555-13_1555-8delinsCTCTTT
NM_012233.2:c.1555-13_1555-8delinsCTCTTT NP_036365.1:n.1555-13_1555-8delinsCTCTTT
XM_011510822.1:c.1555-13_1555-8delinsCTCTTT XP_011509124.1:n.1555-13_1555-8delinsCTCTTT
XM_011510823.1:c.1555-13_1555-8delinsCTCTTT XP_011509125.1:n.1555-13_1555-8delinsCTCTTT
XM_011510824.1:c.1555-13_1555-8delinsCTCTTT XP_011509126.1:n.1555-13_1555-8delinsCTCTTT
XM_011510825.1:c.1555-13_1555-8delinsCTCTTT XP_011509127.1:n.1555-13_1555-8delinsCTCTTT
XM_011510823.3:c.1555-13_1555-8delinsCTCTTT XP_011509125.1:n.1555-13_1555-8delinsCTCTTT
XM_011510825.3:c.1555-13_1555-8delinsCTCTTT XP_011509127.1:n.1555-13_1555-8delinsCTCTTT
XR_001738674.2:n.1582-13_1582-8delinsCTCTTT
NM_001172435.2:c.1555-13_1555-8delinsCTCTTT NP_001165906.1:n.1555-13_1555-8delinsCTCTTT
NM_012233.3:c.1555-13_1555-8delinsCTCTTT MANE Select NP_036365.1:n.1555-13_1555-8delinsCTCTTT