Canonical Allele Identifier: CA2661248788

Gene: RAB3GAP1

Linked Data

• gnomAD v4: 2-135136064-G-GGCGTAAGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135136064_135136065insGCGTAAGCCA , CM000664.2:g.135136064_135136065insGCGTAAGCCA	GRCh38
NC_000002.11:g.135893634_135893635insGCGTAAGCCA , CM000664.1:g.135893634_135893635insGCGTAAGCCA	GRCh37
NC_000002.10:g.135610104_135610105insGCGTAAGCCA	NCBI36
NG_016972.1:g.88800_88801insGCGTAAGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.1923+132_1923+133insGCGTAAGCCA	ENSP00000444306.2:n.1923+132_1923+133insGCGTAAGCCA
ENST00000685967.1:c.*1380+132_*1380+133insGCGTAAGCCA	ENSP00000508423.1:n.*1380+132_*1380+133insGCGTAAGCCA
ENST00000686114.1:n.2269+132_2269+133insGCGTAAGCCA
ENST00000687199.1:c.*1991+132_*1991+133insGCGTAAGCCA	ENSP00000510319.1:n.*1991+132_*1991+133insGCGTAAGCCA
ENST00000688088.1:n.1942+132_1942+133insGCGTAAGCCA
ENST00000688182.1:c.151-31629_151-31628insGCGTAAGCCA	ENSP00000509324.1:n.151-31629_151-31628insGCGTAAGCCA
ENST00000689880.1:n.1942+132_1942+133insGCGTAAGCCA
ENST00000690208.1:c.*1601+132_*1601+133insGCGTAAGCCA	ENSP00000510746.1:n.*1601+132_*1601+133insGCGTAAGCCA
ENST00000690785.1:n.1942+132_1942+133insGCGTAAGCCA
ENST00000691339.1:c.*1546+132_*1546+133insGCGTAAGCCA	ENSP00000509953.1:n.*1546+132_*1546+133insGCGTAAGCCA
ENST00000691478.1:c.*2022+132_*2022+133insGCGTAAGCCA	ENSP00000509081.1:n.*2022+132_*2022+133insGCGTAAGCCA
ENST00000693554.1:c.1923+132_1923+133insGCGTAAGCCA	ENSP00000509030.1:n.1923+132_1923+133insGCGTAAGCCA
ENST00000264158.13:c.1923+132_1923+133insGCGTAAGCCA MANE Select	ENSP00000264158.8:n.1923+132_1923+133insGCGTAAGCCA
ENST00000264158.12:c.1923+132_1923+133insGCGTAAGCCA	ENSP00000264158.7:n.1923+132_1923+133insGCGTAAGCCA
ENST00000442034.5:c.1923+132_1923+133insGCGTAAGCCA	ENSP00000411418.1:n.1923+132_1923+133insGCGTAAGCCA
ENST00000487003.5:n.1992+132_1992+133insGCGTAAGCCA
ENST00000539493.2:c.1791+132_1791+133insGCGTAAGCCA	ENSP00000444306.1:n.1791+132_1791+133insGCGTAAGCCA
NM_001172435.1:c.1923+132_1923+133insGCGTAAGCCA	NP_001165906.1:n.1923+132_1923+133insGCGTAAGCCA
NM_012233.2:c.1923+132_1923+133insGCGTAAGCCA	NP_036365.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510822.1:c.1923+132_1923+133insGCGTAAGCCA	XP_011509124.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510823.1:c.1923+132_1923+133insGCGTAAGCCA	XP_011509125.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510824.1:c.1923+132_1923+133insGCGTAAGCCA	XP_011509126.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510825.1:c.1923+132_1923+133insGCGTAAGCCA	XP_011509127.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510823.3:c.1923+132_1923+133insGCGTAAGCCA	XP_011509125.1:n.1923+132_1923+133insGCGTAAGCCA
XM_011510825.3:c.1923+132_1923+133insGCGTAAGCCA	XP_011509127.1:n.1923+132_1923+133insGCGTAAGCCA
XR_001738674.2:n.1950+132_1950+133insGCGTAAGCCA
NM_001172435.2:c.1923+132_1923+133insGCGTAAGCCA	NP_001165906.1:n.1923+132_1923+133insGCGTAAGCCA
NM_012233.3:c.1923+132_1923+133insGCGTAAGCCA MANE Select	NP_036365.1:n.1923+132_1923+133insGCGTAAGCCA