Canonical Allele Identifier: CA1290542474

Gene: RAB3GAP1 ZRANB3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170178C= , CM000664.2:g.135170178C=	GRCh38
NC_000002.11:g.135927748C= , CM000664.1:g.135927748C=	GRCh37
NC_000002.10:g.135644218C=	NCBI36
NG_016972.1:g.122914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1429C= (RAB3GAP1)	ENSP00000444306.2:n.2914+1429C=
ENST00000685652.1:n.4982C= (RAB3GAP1)
ENST00000685967.1:c.*3800C= (RAB3GAP1)	ENSP00000508423.1:n.*3800C=
ENST00000687199.1:c.*4432C= (RAB3GAP1)	ENSP00000510319.1:n.*4432C=
ENST00000688088.1:n.7525C= (RAB3GAP1)
ENST00000690208.1:c.*4021C= (RAB3GAP1)	ENSP00000510746.1:n.*4021C=
ENST00000691339.1:c.*3987C= (RAB3GAP1)	ENSP00000509953.1:n.*3987C=
ENST00000691478.1:c.*4442C= (RAB3GAP1)	ENSP00000509081.1:n.*4442C=
ENST00000692993.1:n.1922C= (RAB3GAP1)
ENST00000693554.1:c.*2166C= (RAB3GAP1)	ENSP00000509030.1:n.*2166C=
ENST00000264158.13:c.*1397C= (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1397C=
ENST00000264158.12:c.*1397C= (RAB3GAP1)	ENSP00000264158.7:n.*1397C=
ENST00000412849.5:n.1782-5024G= (ZRANB3)
ENST00000487003.5:n.3098+330C= (RAB3GAP1)
ENST00000539493.2:c.2897+330C= (RAB3GAP1)	ENSP00000444306.1:n.2897+330C=
ENST00000619650.4:c.1618-5024G= (ZRANB3)	ENSP00000480120.1:n.1618-5024G=
NM_001172435.1:c.*1397C= (RAB3GAP1)	NP_001165906.1:n.*1397C=
NM_012233.2:c.*1397C= (RAB3GAP1)	NP_036365.1:n.*1397C=
XM_011510822.1:c.2935+1429C= (RAB3GAP1)	XP_011509124.1:n.2935+1429C=
XM_011510823.1:c.2914+1429C= (RAB3GAP1)	XP_011509125.1:n.2914+1429C=
XM_011510824.1:c.*419C= (RAB3GAP1)	XP_011509126.1:n.*419C=
XM_011510825.1:c.*419C= (RAB3GAP1)	XP_011509127.1:n.*419C=
XM_011510823.3:c.2914+1429C= (RAB3GAP1)	XP_011509125.1:n.2914+1429C=
XM_011510825.3:c.*419C= (RAB3GAP1)	XP_011509127.1:n.*419C=
XM_011511966.3:c.3049-5024G= (ZRANB3)	XP_011510268.2:n.3049-5024G=
XR_001738674.2:n.2941+1429C= (RAB3GAP1)
NM_001172435.2:c.*1397C= (RAB3GAP1)	NP_001165906.1:n.*1397C=
NM_012233.3:c.*1397C= (RAB3GAP1) MANE Select	NP_036365.1:n.*1397C=