Canonical Allele Identifier: CA1290526728

Gene: RAB3GAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135132891C= , CM000664.2:g.135132891C=	GRCh38
NC_000002.11:g.135890461C= , CM000664.1:g.135890461C=	GRCh37
NC_000002.10:g.135606931C=	NCBI36
NG_016972.1:g.85627C=

Transcript Alleles

HGVS	Amino-acid Change
NM_012233.3:c.1237-4C= MANE Select	NP_036365.1:n.1237-4C=
ENST00000264158.13:c.1237-4C= MANE Select	ENSP00000264158.8:n.1237-4C=
NM_001172435.1:c.1237-4C=	NP_001165906.1:n.1237-4C=
NM_001172435.2:c.1237-4C=	NP_001165906.1:n.1237-4C=
NM_012233.2:c.1237-4C=	NP_036365.1:n.1237-4C=
ENST00000264158.12:c.1237-4C=	ENSP00000264158.7:n.1237-4C=
ENST00000442034.5:c.1237-4C=	ENSP00000411418.1:n.1237-4C=
ENST00000487003.5:n.1306-4C=
ENST00000539493.2:c.1105-4C=	ENSP00000444306.1:n.1105-4C=
ENST00000539493.3:c.1237-4C=	ENSP00000444306.2:n.1237-4C=
ENST00000685967.1:c.*694-4C=	ENSP00000508423.1:n.*694-4C=
ENST00000686114.1:n.1583-4C=
ENST00000687199.1:c.*1305-4C=	ENSP00000510319.1:n.*1305-4C=
ENST00000688088.1:n.1256-4C=
ENST00000688182.1:c.151-34802C=	ENSP00000509324.1:n.151-34802C=
ENST00000689880.1:n.1256-4C=
ENST00000690208.1:c.*915-4C=	ENSP00000510746.1:n.*915-4C=
ENST00000690785.1:n.1256-4C=
ENST00000691339.1:c.*860-4C=	ENSP00000509953.1:n.*860-4C=
ENST00000691478.1:c.*1336-4C=	ENSP00000509081.1:n.*1336-4C=
ENST00000693554.1:c.1237-4C=	ENSP00000509030.1:n.1237-4C=
XM_011510822.1:c.1237-4C=	XP_011509124.1:n.1237-4C=
XM_011510823.1:c.1237-4C=	XP_011509125.1:n.1237-4C=
XM_011510823.3:c.1237-4C=	XP_011509125.1:n.1237-4C=
XM_011510824.1:c.1237-4C=	XP_011509126.1:n.1237-4C=
XM_011510825.1:c.1237-4C=	XP_011509127.1:n.1237-4C=
XM_011510825.3:c.1237-4C=	XP_011509127.1:n.1237-4C=
XR_001738674.2:n.1264-4C=