Canonical Allele Identifier: CA1290523765

Gene: RAB3GAP1

Linked Data

• dbSNP Id: rs1691345748
• gnomAD v4: 2-135126266-T-TAGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135126267_135126270dup , CM000664.2:g.135126267_135126270dup	GRCh38
NC_000002.11:g.135883837_135883840dup , CM000664.1:g.135883837_135883840dup	GRCh37
NC_000002.10:g.135600307_135600310dup	NCBI36
NG_016972.1:g.79003_79006dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000539493.3:c.899+18_899+21dup	ENSP00000444306.2:n.899+18_899+21dup
ENST00000685967.1:c.*356+18_*356+21dup	ENSP00000508423.1:n.*356+18_*356+21dup
ENST00000686114.1:n.930_933dup
ENST00000687199.1:c.*967+18_*967+21dup	ENSP00000510319.1:n.*967+18_*967+21dup
ENST00000688088.1:n.918+18_918+21dup
ENST00000688182.1:c.151-41426_151-41423dup	ENSP00000509324.1:n.151-41426_151-41423du...
ENST00000689880.1:n.918+18_918+21dup
ENST00000690208.1:c.*577+18_*577+21dup	ENSP00000510746.1:n.*577+18_*577+21dup
ENST00000690785.1:n.918+18_918+21dup
ENST00000691339.1:c.*522+18_*522+21dup	ENSP00000509953.1:n.*522+18_*522+21dup
ENST00000691478.1:c.*998+18_*998+21dup	ENSP00000509081.1:n.*998+18_*998+21dup
ENST00000693554.1:c.899+18_899+21dup	ENSP00000509030.1:n.899+18_899+21dup
ENST00000264158.13:c.899+18_899+21dup MANE Select	ENSP00000264158.8:n.899+18_899+21dup
ENST00000264158.12:c.899+18_899+21dup	ENSP00000264158.7:n.899+18_899+21dup
ENST00000442034.5:c.899+18_899+21dup	ENSP00000411418.1:n.899+18_899+21dup
ENST00000487003.5:n.968+18_968+21dup
ENST00000489858.1:n.236+18_236+21dup
ENST00000539493.2:c.767+18_767+21dup	ENSP00000444306.1:n.767+18_767+21dup
NM_001172435.1:c.899+18_899+21dup	NP_001165906.1:n.899+18_899+21dup
NM_012233.2:c.899+18_899+21dup	NP_036365.1:n.899+18_899+21dup
XM_011510822.1:c.899+18_899+21dup	XP_011509124.1:n.899+18_899+21dup
XM_011510823.1:c.899+18_899+21dup	XP_011509125.1:n.899+18_899+21dup
XM_011510824.1:c.899+18_899+21dup	XP_011509126.1:n.899+18_899+21dup
XM_011510825.1:c.899+18_899+21dup	XP_011509127.1:n.899+18_899+21dup
XM_011510823.3:c.899+18_899+21dup	XP_011509125.1:n.899+18_899+21dup
XM_011510825.3:c.899+18_899+21dup	XP_011509127.1:n.899+18_899+21dup
XR_001738674.2:n.926+18_926+21dup
NM_001172435.2:c.899+18_899+21dup	NP_001165906.1:n.899+18_899+21dup
NM_012233.3:c.899+18_899+21dup MANE Select	NP_036365.1:n.899+18_899+21dup