Canonical Allele Identifier: CA1290542473

Gene: RAB3GAP1 ZRANB3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170176G= , CM000664.2:g.135170176G=	GRCh38
NC_000002.11:g.135927746G= , CM000664.1:g.135927746G=	GRCh37
NC_000002.10:g.135644216G=	NCBI36
NG_016972.1:g.122912G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1427G= (RAB3GAP1)	ENSP00000444306.2:n.2914+1427G=
ENST00000685652.1:n.4980G= (RAB3GAP1)
ENST00000685967.1:c.*3798G= (RAB3GAP1)	ENSP00000508423.1:n.*3798G=
ENST00000687199.1:c.*4430G= (RAB3GAP1)	ENSP00000510319.1:n.*4430G=
ENST00000688088.1:n.7523G= (RAB3GAP1)
ENST00000690208.1:c.*4019G= (RAB3GAP1)	ENSP00000510746.1:n.*4019G=
ENST00000691339.1:c.*3985G= (RAB3GAP1)	ENSP00000509953.1:n.*3985G=
ENST00000691478.1:c.*4440G= (RAB3GAP1)	ENSP00000509081.1:n.*4440G=
ENST00000692993.1:n.1920G= (RAB3GAP1)
ENST00000693554.1:c.*2164G= (RAB3GAP1)	ENSP00000509030.1:n.*2164G=
ENST00000264158.13:c.*1395G= (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1395G=
ENST00000264158.12:c.*1395G= (RAB3GAP1)	ENSP00000264158.7:n.*1395G=
ENST00000412849.5:n.1782-5022C= (ZRANB3)
ENST00000487003.5:n.3098+328G= (RAB3GAP1)
ENST00000539493.2:c.2897+328G= (RAB3GAP1)	ENSP00000444306.1:n.2897+328G=
ENST00000619650.4:c.1618-5022C= (ZRANB3)	ENSP00000480120.1:n.1618-5022C=
NM_001172435.1:c.*1395G= (RAB3GAP1)	NP_001165906.1:n.*1395G=
NM_012233.2:c.*1395G= (RAB3GAP1)	NP_036365.1:n.*1395G=
XM_011510822.1:c.2935+1427G= (RAB3GAP1)	XP_011509124.1:n.2935+1427G=
XM_011510823.1:c.2914+1427G= (RAB3GAP1)	XP_011509125.1:n.2914+1427G=
XM_011510824.1:c.*417G= (RAB3GAP1)	XP_011509126.1:n.*417G=
XM_011510825.1:c.*417G= (RAB3GAP1)	XP_011509127.1:n.*417G=
XM_011510823.3:c.2914+1427G= (RAB3GAP1)	XP_011509125.1:n.2914+1427G=
XM_011510825.3:c.*417G= (RAB3GAP1)	XP_011509127.1:n.*417G=
XM_011511966.3:c.3049-5022C= (ZRANB3)	XP_011510268.2:n.3049-5022C=
XR_001738674.2:n.2941+1427G= (RAB3GAP1)
NM_001172435.2:c.*1395G= (RAB3GAP1)	NP_001165906.1:n.*1395G=
NM_012233.3:c.*1395G= (RAB3GAP1) MANE Select	NP_036365.1:n.*1395G=