Canonical Allele Identifier: CA1290542476
Gene: RAB3GAP1 HGNC NCBI
ZRANB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135170183C= , CM000664.2:g.135170183C= GRCh38
NC_000002.11:g.135927753C= , CM000664.1:g.135927753C= GRCh37
NC_000002.10:g.135644223C= NCBI36
NG_016972.1:g.122919C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.2914+1434C= (RAB3GAP1) ENSP00000444306.2:n.2914+1434C=
ENST00000685652.1:n.4987C= (RAB3GAP1)
ENST00000685967.1:c.*3805C= (RAB3GAP1) ENSP00000508423.1:n.*3805C=
ENST00000687199.1:c.*4437C= (RAB3GAP1) ENSP00000510319.1:n.*4437C=
ENST00000688088.1:n.7530C= (RAB3GAP1)
ENST00000690208.1:c.*4026C= (RAB3GAP1) ENSP00000510746.1:n.*4026C=
ENST00000691339.1:c.*3992C= (RAB3GAP1) ENSP00000509953.1:n.*3992C=
ENST00000691478.1:c.*4447C= (RAB3GAP1) ENSP00000509081.1:n.*4447C=
ENST00000692993.1:n.1927C= (RAB3GAP1)
ENST00000693554.1:c.*2171C= (RAB3GAP1) ENSP00000509030.1:n.*2171C=
ENST00000264158.13:c.*1402C= (RAB3GAP1) MANE Select ENSP00000264158.8:n.*1402C=
ENST00000264158.12:c.*1402C= (RAB3GAP1) ENSP00000264158.7:n.*1402C=
ENST00000412849.5:n.1782-5029G= (ZRANB3)
ENST00000487003.5:n.3098+335C= (RAB3GAP1)
ENST00000539493.2:c.2897+335C= (RAB3GAP1) ENSP00000444306.1:n.2897+335C=
ENST00000619650.4:c.1618-5029G= (ZRANB3) ENSP00000480120.1:n.1618-5029G=
NM_001172435.1:c.*1402C= (RAB3GAP1) NP_001165906.1:n.*1402C=
NM_012233.2:c.*1402C= (RAB3GAP1) NP_036365.1:n.*1402C=
XM_011510822.1:c.2935+1434C= (RAB3GAP1) XP_011509124.1:n.2935+1434C=
XM_011510823.1:c.2914+1434C= (RAB3GAP1) XP_011509125.1:n.2914+1434C=
XM_011510824.1:c.*424C= (RAB3GAP1) XP_011509126.1:n.*424C=
XM_011510825.1:c.*424C= (RAB3GAP1) XP_011509127.1:n.*424C=
XM_011510823.3:c.2914+1434C= (RAB3GAP1) XP_011509125.1:n.2914+1434C=
XM_011510825.3:c.*424C= (RAB3GAP1) XP_011509127.1:n.*424C=
XM_011511966.3:c.3049-5029G= (ZRANB3) XP_011510268.2:n.3049-5029G=
XR_001738674.2:n.2941+1434C= (RAB3GAP1)
NM_001172435.2:c.*1402C= (RAB3GAP1) NP_001165906.1:n.*1402C=
NM_012233.3:c.*1402C= (RAB3GAP1) MANE Select NP_036365.1:n.*1402C=