Canonical Allele Identifier: CA1290542472

Gene: RAB3GAP1 ZRANB3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135170172_135170173insT , CM000664.2:g.135170172_135170173insT	GRCh38
NC_000002.11:g.135927742_135927743insT , CM000664.1:g.135927742_135927743insT	GRCh37
NC_000002.10:g.135644212_135644213insT	NCBI36
NG_016972.1:g.122908_122909insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.2914+1423_2914+1424insT (RAB3GAP1)	ENSP00000444306.2:n.2914+1423_2914+1424insT
ENST00000685652.1:n.4976_4977insT (RAB3GAP1)
ENST00000685967.1:c.*3794_*3795insT (RAB3GAP1)	ENSP00000508423.1:n.*3794_*3795insT
ENST00000687199.1:c.*4426_*4427insT (RAB3GAP1)	ENSP00000510319.1:n.*4426_*4427insT
ENST00000688088.1:n.7519_7520insT (RAB3GAP1)
ENST00000690208.1:c.*4015_*4016insT (RAB3GAP1)	ENSP00000510746.1:n.*4015_*4016insT
ENST00000691339.1:c.*3981_*3982insT (RAB3GAP1)	ENSP00000509953.1:n.*3981_*3982insT
ENST00000691478.1:c.*4436_*4437insT (RAB3GAP1)	ENSP00000509081.1:n.*4436_*4437insT
ENST00000692993.1:n.1916_1917insT (RAB3GAP1)
ENST00000693554.1:c.*2160_*2161insT (RAB3GAP1)	ENSP00000509030.1:n.*2160_*2161insT
ENST00000264158.13:c.*1391_*1392insT (RAB3GAP1) MANE Select	ENSP00000264158.8:n.*1391_*1392insT
ENST00000264158.12:c.*1391_*1392insT (RAB3GAP1)	ENSP00000264158.7:n.*1391_*1392insT
ENST00000412849.5:n.1782-5019_1782-5018insA (ZRANB3)
ENST00000487003.5:n.3098+324_3098+325insT (RAB3GAP1)
ENST00000539493.2:c.2897+324_2897+325insT (RAB3GAP1)	ENSP00000444306.1:n.2897+324_2897+325insT
ENST00000619650.4:c.1618-5019_1618-5018insA (ZRANB3)	ENSP00000480120.1:n.1618-5019_1618-5018insA
NM_001172435.1:c.*1391_*1392insT (RAB3GAP1)	NP_001165906.1:n.*1391_*1392insT
NM_012233.2:c.*1391_*1392insT (RAB3GAP1)	NP_036365.1:n.*1391_*1392insT
XM_011510822.1:c.2935+1423_2935+1424insT (RAB3GAP1)	XP_011509124.1:n.2935+1423_2935+1424insT
XM_011510823.1:c.2914+1423_2914+1424insT (RAB3GAP1)	XP_011509125.1:n.2914+1423_2914+1424insT
XM_011510824.1:c.*413_*414insT (RAB3GAP1)	XP_011509126.1:n.*413_*414insT
XM_011510825.1:c.*413_*414insT (RAB3GAP1)	XP_011509127.1:n.*413_*414insT
XM_011510823.3:c.2914+1423_2914+1424insT (RAB3GAP1)	XP_011509125.1:n.2914+1423_2914+1424insT
XM_011510825.3:c.*413_*414insT (RAB3GAP1)	XP_011509127.1:n.*413_*414insT
XM_011511966.3:c.3049-5019_3049-5018insA (ZRANB3)	XP_011510268.2:n.3049-5019_3049-5018insA
XR_001738674.2:n.2941+1423_2941+1424insT (RAB3GAP1)
NM_001172435.2:c.*1391_*1392insT (RAB3GAP1)	NP_001165906.1:n.*1391_*1392insT
NM_012233.3:c.*1391_*1392insT (RAB3GAP1) MANE Select	NP_036365.1:n.*1391_*1392insT