Canonical Allele Identifier: CA1884884

Gene: RAB3GAP1

Linked Data

• dbSNP Id: rs761297819
• ExAC: 2:135893097 C / T
• gnomAD v2: 2-135893097-C-T
• gnomAD v4: 2-135135527-C-T
• MyVariant Identifiers: chr2:g.135893097C>T (hg19) ; chr2:g.135135527C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135135527C>T , CM000664.2:g.135135527C>T	GRCh38
NC_000002.11:g.135893097C>T , CM000664.1:g.135893097C>T	GRCh37
NC_000002.10:g.135609567C>T	NCBI36
NG_016972.1:g.88263C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539493.3:c.1555-37C>T	ENSP00000444306.2:n.1555-37C>T
ENST00000685967.1:c.*1012-37C>T	ENSP00000508423.1:n.*1012-37C>T
ENST00000686114.1:n.1901-37C>T
ENST00000687199.1:c.*1623-37C>T	ENSP00000510319.1:n.*1623-37C>T
ENST00000688088.1:n.1574-37C>T
ENST00000688182.1:c.151-32166C>T	ENSP00000509324.1:n.151-32166C>T
ENST00000689880.1:n.1574-37C>T
ENST00000690208.1:c.*1233-37C>T	ENSP00000510746.1:n.*1233-37C>T
ENST00000690785.1:n.1574-37C>T
ENST00000691339.1:c.*1178-37C>T	ENSP00000509953.1:n.*1178-37C>T
ENST00000691478.1:c.*1654-37C>T	ENSP00000509081.1:n.*1654-37C>T
ENST00000693554.1:c.1555-37C>T	ENSP00000509030.1:n.1555-37C>T
ENST00000264158.13:c.1555-37C>T MANE Select	ENSP00000264158.8:n.1555-37C>T
ENST00000264158.12:c.1555-37C>T	ENSP00000264158.7:n.1555-37C>T
ENST00000442034.5:c.1555-37C>T	ENSP00000411418.1:n.1555-37C>T
ENST00000487003.5:n.1624-37C>T
ENST00000539493.2:c.1423-37C>T	ENSP00000444306.1:n.1423-37C>T
NM_001172435.1:c.1555-37C>T	NP_001165906.1:n.1555-37C>T
NM_012233.2:c.1555-37C>T	NP_036365.1:n.1555-37C>T
XM_011510822.1:c.1555-37C>T	XP_011509124.1:n.1555-37C>T
XM_011510823.1:c.1555-37C>T	XP_011509125.1:n.1555-37C>T
XM_011510824.1:c.1555-37C>T	XP_011509126.1:n.1555-37C>T
XM_011510825.1:c.1555-37C>T	XP_011509127.1:n.1555-37C>T
XM_011510823.3:c.1555-37C>T	XP_011509125.1:n.1555-37C>T
XM_011510825.3:c.1555-37C>T	XP_011509127.1:n.1555-37C>T
XR_001738674.2:n.1582-37C>T
NM_001172435.2:c.1555-37C>T	NP_001165906.1:n.1555-37C>T
NM_012233.3:c.1555-37C>T MANE Select	NP_036365.1:n.1555-37C>T