Canonical Allele Identifier: CA1290518852

Gene: RAB3GAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135115366C= , CM000664.2:g.135115366C=	GRCh38
NC_000002.11:g.135872936C= , CM000664.1:g.135872936C=	GRCh37
NC_000002.10:g.135589406C=	NCBI36
NG_016972.1:g.68102C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.633C=	ENSP00000444306.2:p.Ile211=
ENST00000685967.1:c.*105+2096C=	ENSP00000508423.1:n.*105+2096C=
ENST00000686114.1:n.646C=
ENST00000687199.1:c.*701C=	ENSP00000510319.1:n.*701C=
ENST00000688088.1:n.652C=
ENST00000688182.1:c.151-52327C=	ENSP00000509324.1:n.151-52327C=
ENST00000689880.1:n.652C=
ENST00000690208.1:c.*311C=	ENSP00000510746.1:n.*311C=
ENST00000690785.1:n.652C=
ENST00000691339.1:c.*256C=	ENSP00000509953.1:n.*256C=
ENST00000691478.1:c.*732C=	ENSP00000509081.1:n.*732C=
ENST00000693554.1:c.633C=	ENSP00000509030.1:p.Ile211=
ENST00000264158.13:c.633C= MANE Select	ENSP00000264158.8:p.Ile211=
ENST00000264158.12:c.633C=	ENSP00000264158.7:p.Ile211=
ENST00000442034.5:c.633C=	ENSP00000411418.1:p.Ile211=
ENST00000487003.5:n.702C=
ENST00000539493.2:c.501C=	ENSP00000444306.1:p.Ile167=
NM_001172435.1:c.633C=	NP_001165906.1:p.Ile211=
NM_012233.2:c.633C=	NP_036365.1:p.Ile211=
XM_011510822.1:c.633C=	XP_011509124.1:p.Ile211=
XM_011510823.1:c.633C=	XP_011509125.1:p.Ile211=
XM_011510824.1:c.633C=	XP_011509126.1:p.Ile211=
XM_011510825.1:c.633C=	XP_011509127.1:p.Ile211=
XM_011510823.3:c.633C=	XP_011509125.1:p.Ile211=
XM_011510825.3:c.633C=	XP_011509127.1:p.Ile211=
XR_001738674.2:n.660C=
NM_001172435.2:c.633C=	NP_001165906.1:p.Ile211=
NM_012233.3:c.633C= MANE Select	NP_036365.1:p.Ile211=