Canonical Allele Identifier: CA2586969889

Gene: RAB3GAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135126251dup , CM000664.2:g.135126251dup	GRCh38
NC_000002.11:g.135883821dup , CM000664.1:g.135883821dup	GRCh37
NC_000002.10:g.135600291dup	NCBI36
NG_016972.1:g.78987dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000539493.3:c.899+2dup	ENSP00000444306.2:n.899+2dup
ENST00000685967.1:c.*356+2dup	ENSP00000508423.1:n.*356+2dup
ENST00000686114.1:n.914dup
ENST00000687199.1:c.*967+2dup	ENSP00000510319.1:n.*967+2dup
ENST00000688088.1:n.918+2dup
ENST00000688182.1:c.151-41442dup	ENSP00000509324.1:n.151-41442dup
ENST00000689880.1:n.918+2dup
ENST00000690208.1:c.*577+2dup	ENSP00000510746.1:n.*577+2dup
ENST00000690785.1:n.918+2dup
ENST00000691339.1:c.*522+2dup	ENSP00000509953.1:n.*522+2dup
ENST00000691478.1:c.*998+2dup	ENSP00000509081.1:n.*998+2dup
ENST00000693554.1:c.899+2dup	ENSP00000509030.1:n.899+2dup
ENST00000264158.13:c.899+2dup MANE Select	ENSP00000264158.8:n.899+2dup
ENST00000264158.12:c.899+2dup	ENSP00000264158.7:n.899+2dup
ENST00000442034.5:c.899+2dup	ENSP00000411418.1:n.899+2dup
ENST00000487003.5:n.968+2dup
ENST00000489858.1:n.236+2dup
ENST00000539493.2:c.767+2dup	ENSP00000444306.1:n.767+2dup
NM_001172435.1:c.899+2dup	NP_001165906.1:n.899+2dup
NM_012233.2:c.899+2dup	NP_036365.1:n.899+2dup
XM_011510822.1:c.899+2dup	XP_011509124.1:n.899+2dup
XM_011510823.1:c.899+2dup	XP_011509125.1:n.899+2dup
XM_011510824.1:c.899+2dup	XP_011509126.1:n.899+2dup
XM_011510825.1:c.899+2dup	XP_011509127.1:n.899+2dup
XM_011510823.3:c.899+2dup	XP_011509125.1:n.899+2dup
XM_011510825.3:c.899+2dup	XP_011509127.1:n.899+2dup
XR_001738674.2:n.926+2dup
NM_001172435.2:c.899+2dup	NP_001165906.1:n.899+2dup
NM_012233.3:c.899+2dup MANE Select	NP_036365.1:n.899+2dup