Canonical Allele Identifier: CA2661250822

Gene: RAB3GAP1 ZRANB3

Linked Data

• gnomAD v4: 2-135170071-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170071A>G , CM000664.2:g.135170071A>G	GRCh38
NC_000002.11:g.135927641A>G , CM000664.1:g.135927641A>G	GRCh37
NC_000002.10:g.135644111A>G	NCBI36
NG_016972.1:g.122807A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1322A>G (RAB3GAP1)	ENSP00000444306.2:n.2914+1322A>G
ENST00000685652.1:n.4875A>G (RAB3GAP1)
ENST00000685967.1:c.*3693A>G (RAB3GAP1)	ENSP00000508423.1:n.*3693A>G
ENST00000687199.1:c.*4325A>G (RAB3GAP1)	ENSP00000510319.1:n.*4325A>G
ENST00000688088.1:n.7418A>G (RAB3GAP1)
ENST00000688182.1:c.1698A>G (RAB3GAP1)	ENSP00000509324.1:n.1698A>G
ENST00000690208.1:c.*3914A>G (RAB3GAP1)	ENSP00000510746.1:n.*3914A>G
ENST00000691339.1:c.*3880A>G (RAB3GAP1)	ENSP00000509953.1:n.*3880A>G
ENST00000691478.1:c.*4335A>G (RAB3GAP1)	ENSP00000509081.1:n.*4335A>G
ENST00000692993.1:n.1815A>G (RAB3GAP1)
ENST00000693554.1:c.*2059A>G (RAB3GAP1)	ENSP00000509030.1:n.*2059A>G
ENST00000264158.13:c.*1290A>G (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1290A>G
ENST00000264158.12:c.*1290A>G (RAB3GAP1)	ENSP00000264158.7:n.*1290A>G
ENST00000412849.5:n.1782-4917T>C (ZRANB3)
ENST00000487003.5:n.3098+223A>G (RAB3GAP1)
ENST00000539493.2:c.2897+223A>G (RAB3GAP1)	ENSP00000444306.1:n.2897+223A>G
ENST00000619650.4:c.1618-4917T>C (ZRANB3)	ENSP00000480120.1:n.1618-4917T>C
NM_001172435.1:c.*1290A>G (RAB3GAP1)	NP_001165906.1:n.*1290A>G
NM_012233.2:c.*1290A>G (RAB3GAP1)	NP_036365.1:n.*1290A>G
XM_011510822.1:c.2935+1322A>G (RAB3GAP1)	XP_011509124.1:n.2935+1322A>G
XM_011510823.1:c.2914+1322A>G (RAB3GAP1)	XP_011509125.1:n.2914+1322A>G
XM_011510824.1:c.*312A>G (RAB3GAP1)	XP_011509126.1:n.*312A>G
XM_011510825.1:c.*312A>G (RAB3GAP1)	XP_011509127.1:n.*312A>G
XM_011510823.3:c.2914+1322A>G (RAB3GAP1)	XP_011509125.1:n.2914+1322A>G
XM_011510825.3:c.*312A>G (RAB3GAP1)	XP_011509127.1:n.*312A>G
XM_011511966.3:c.3049-4917T>C (ZRANB3)	XP_011510268.2:n.3049-4917T>C
XR_001738674.2:n.2941+1322A>G (RAB3GAP1)
NM_001172435.2:c.*1290A>G (RAB3GAP1)	NP_001165906.1:n.*1290A>G
NM_012233.3:c.*1290A>G (RAB3GAP1) MANE Select	NP_036365.1:n.*1290A>G