Canonical Allele Identifier: CA1290542471

Gene: RAB3GAP1 ZRANB3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170173G= , CM000664.2:g.135170173G=	GRCh38
NC_000002.11:g.135927743G= , CM000664.1:g.135927743G=	GRCh37
NC_000002.10:g.135644213G=	NCBI36
NG_016972.1:g.122909G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1424G= (RAB3GAP1)	ENSP00000444306.2:n.2914+1424G=
ENST00000685652.1:n.4977G= (RAB3GAP1)
ENST00000685967.1:c.*3795G= (RAB3GAP1)	ENSP00000508423.1:n.*3795G=
ENST00000687199.1:c.*4427G= (RAB3GAP1)	ENSP00000510319.1:n.*4427G=
ENST00000688088.1:n.7520G= (RAB3GAP1)
ENST00000690208.1:c.*4016G= (RAB3GAP1)	ENSP00000510746.1:n.*4016G=
ENST00000691339.1:c.*3982G= (RAB3GAP1)	ENSP00000509953.1:n.*3982G=
ENST00000691478.1:c.*4437G= (RAB3GAP1)	ENSP00000509081.1:n.*4437G=
ENST00000692993.1:n.1917G= (RAB3GAP1)
ENST00000693554.1:c.*2161G= (RAB3GAP1)	ENSP00000509030.1:n.*2161G=
ENST00000264158.13:c.*1392G= (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1392G=
ENST00000264158.12:c.*1392G= (RAB3GAP1)	ENSP00000264158.7:n.*1392G=
ENST00000412849.5:n.1782-5019C= (ZRANB3)
ENST00000487003.5:n.3098+325G= (RAB3GAP1)
ENST00000539493.2:c.2897+325G= (RAB3GAP1)	ENSP00000444306.1:n.2897+325G=
ENST00000619650.4:c.1618-5019C= (ZRANB3)	ENSP00000480120.1:n.1618-5019C=
NM_001172435.1:c.*1392G= (RAB3GAP1)	NP_001165906.1:n.*1392G=
NM_012233.2:c.*1392G= (RAB3GAP1)	NP_036365.1:n.*1392G=
XM_011510822.1:c.2935+1424G= (RAB3GAP1)	XP_011509124.1:n.2935+1424G=
XM_011510823.1:c.2914+1424G= (RAB3GAP1)	XP_011509125.1:n.2914+1424G=
XM_011510824.1:c.*414G= (RAB3GAP1)	XP_011509126.1:n.*414G=
XM_011510825.1:c.*414G= (RAB3GAP1)	XP_011509127.1:n.*414G=
XM_011510823.3:c.2914+1424G= (RAB3GAP1)	XP_011509125.1:n.2914+1424G=
XM_011510825.3:c.*414G= (RAB3GAP1)	XP_011509127.1:n.*414G=
XM_011511966.3:c.3049-5019C= (ZRANB3)	XP_011510268.2:n.3049-5019C=
XR_001738674.2:n.2941+1424G= (RAB3GAP1)
NM_001172435.2:c.*1392G= (RAB3GAP1)	NP_001165906.1:n.*1392G=
NM_012233.3:c.*1392G= (RAB3GAP1) MANE Select	NP_036365.1:n.*1392G=