Canonical Allele Identifier: CA56568775

Gene: RAB3GAP1

Linked Data

• dbSNP Id: rs982380101
• gnomAD v2: 2-135872941-A-G
• gnomAD v4: 2-135115371-A-G
• MyVariant Identifiers: chr2:g.135872941A>G (hg19) ; chr2:g.135115371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135115371A>G , CM000664.2:g.135115371A>G	GRCh38
NC_000002.11:g.135872941A>G , CM000664.1:g.135872941A>G	GRCh37
NC_000002.10:g.135589411A>G	NCBI36
NG_016972.1:g.68107A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.638A>G	ENSP00000444306.2:p.Lys213Arg
ENST00000685967.1:c.*105+2101A>G	ENSP00000508423.1:n.*105+2101A>G
ENST00000686114.1:n.651A>G
ENST00000687199.1:c.*706A>G	ENSP00000510319.1:n.*706A>G
ENST00000688088.1:n.657A>G
ENST00000688182.1:c.151-52322A>G	ENSP00000509324.1:n.151-52322A>G
ENST00000689880.1:n.657A>G
ENST00000690208.1:c.*316A>G	ENSP00000510746.1:n.*316A>G
ENST00000690785.1:n.657A>G
ENST00000691339.1:c.*261A>G	ENSP00000509953.1:n.*261A>G
ENST00000691478.1:c.*737A>G	ENSP00000509081.1:n.*737A>G
ENST00000693554.1:c.638A>G	ENSP00000509030.1:p.Lys213Arg
ENST00000264158.13:c.638A>G MANE Select	ENSP00000264158.8:p.Lys213Arg
ENST00000264158.12:c.638A>G	ENSP00000264158.7:p.Lys213Arg
ENST00000442034.5:c.638A>G	ENSP00000411418.1:p.Lys213Arg
ENST00000487003.5:n.707A>G
ENST00000539493.2:c.506A>G	ENSP00000444306.1:p.Lys169Arg
NM_001172435.1:c.638A>G	NP_001165906.1:p.Lys213Arg
NM_012233.2:c.638A>G	NP_036365.1:p.Lys213Arg
XM_011510822.1:c.638A>G	XP_011509124.1:p.Lys213Arg
XM_011510823.1:c.638A>G	XP_011509125.1:p.Lys213Arg
XM_011510824.1:c.638A>G	XP_011509126.1:p.Lys213Arg
XM_011510825.1:c.638A>G	XP_011509127.1:p.Lys213Arg
XM_011510823.3:c.638A>G	XP_011509125.1:p.Lys213Arg
XM_011510825.3:c.638A>G	XP_011509127.1:p.Lys213Arg
XR_001738674.2:n.665A>G
NM_001172435.2:c.638A>G	NP_001165906.1:p.Lys213Arg
NM_012233.3:c.638A>G MANE Select	NP_036365.1:p.Lys213Arg