Canonical Allele Identifier: CA757383857

Gene: RAB3GAP1 ZRANB3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170168_135170175del , CM000664.2:g.135170168_135170175del	GRCh38
NC_000002.11:g.135927738_135927745del , CM000664.1:g.135927738_135927745del	GRCh37
NC_000002.10:g.135644208_135644215del	NCBI36
NG_016972.1:g.122904_122911del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1419_2914+1426del (RAB3GAP1)	ENSP00000444306.2:n.2914+1419_2914+1426del
ENST00000685652.1:n.4972_4979del (RAB3GAP1)
ENST00000685967.1:c.*3790_*3797del (RAB3GAP1)	ENSP00000508423.1:n.*3790_*3797del
ENST00000687199.1:c.*4422_*4429del (RAB3GAP1)	ENSP00000510319.1:n.*4422_*4429del
ENST00000688088.1:n.7515_7522del (RAB3GAP1)
ENST00000690208.1:c.*4011_*4018del (RAB3GAP1)	ENSP00000510746.1:n.*4011_*4018del
ENST00000691339.1:c.*3977_*3984del (RAB3GAP1)	ENSP00000509953.1:n.*3977_*3984del
ENST00000691478.1:c.*4432_*4439del (RAB3GAP1)	ENSP00000509081.1:n.*4432_*4439del
ENST00000692993.1:n.1912_1919del (RAB3GAP1)
ENST00000693554.1:c.*2156_*2163del (RAB3GAP1)	ENSP00000509030.1:n.*2156_*2163del
ENST00000264158.13:c.*1387_*1394del (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1387_*1394del
ENST00000264158.12:c.*1387_*1394del (RAB3GAP1)	ENSP00000264158.7:n.*1387_*1394del
ENST00000412849.5:n.1782-5021_1782-5014del (ZRANB3)
ENST00000487003.5:n.3098+320_3098+327del (RAB3GAP1)
ENST00000539493.2:c.2897+320_2897+327del (RAB3GAP1)	ENSP00000444306.1:n.2897+320_2897+327del
ENST00000619650.4:c.1618-5021_1618-5014del (ZRANB3)	ENSP00000480120.1:n.1618-5021_1618-5014del
NM_001172435.1:c.*1387_*1394del (RAB3GAP1)	NP_001165906.1:n.*1387_*1394del
NM_012233.2:c.*1387_*1394del (RAB3GAP1)	NP_036365.1:n.*1387_*1394del
XM_011510822.1:c.2935+1419_2935+1426del (RAB3GAP1)	XP_011509124.1:n.2935+1419_2935+1426del
XM_011510823.1:c.2914+1419_2914+1426del (RAB3GAP1)	XP_011509125.1:n.2914+1419_2914+1426del
XM_011510824.1:c.*409_*416del (RAB3GAP1)	XP_011509126.1:n.*409_*416del
XM_011510825.1:c.*409_*416del (RAB3GAP1)	XP_011509127.1:n.*409_*416del
XM_011510823.3:c.2914+1419_2914+1426del (RAB3GAP1)	XP_011509125.1:n.2914+1419_2914+1426del
XM_011510825.3:c.*409_*416del (RAB3GAP1)	XP_011509127.1:n.*409_*416del
XM_011511966.3:c.3049-5021_3049-5014del (ZRANB3)	XP_011510268.2:n.3049-5021_3049-5014del
XR_001738674.2:n.2941+1419_2941+1426del (RAB3GAP1)
NM_001172435.2:c.*1387_*1394del (RAB3GAP1)	NP_001165906.1:n.*1387_*1394del
NM_012233.3:c.*1387_*1394del (RAB3GAP1) MANE Select	NP_036365.1:n.*1387_*1394del