Canonical Allele Identifier: CA56588551
Gene: RAB3GAP1 HGNC NCBI
ZRANB3 HGNC NCBI

Linked Data

dbSNP Id: rs557776134

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135170083C>T , CM000664.2:g.135170083C>T GRCh38
NC_000002.11:g.135927653C>T , CM000664.1:g.135927653C>T GRCh37
NC_000002.10:g.135644123C>T NCBI36
NG_016972.1:g.122819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000539493.3:c.2914+1334C>T (RAB3GAP1) ENSP00000444306.2:n.2914+1334C>T
ENST00000685652.1:n.4887C>T (RAB3GAP1)
ENST00000685967.1:c.*3705C>T (RAB3GAP1) ENSP00000508423.1:n.*3705C>T
ENST00000687199.1:c.*4337C>T (RAB3GAP1) ENSP00000510319.1:n.*4337C>T
ENST00000688088.1:n.7430C>T (RAB3GAP1)
ENST00000690208.1:c.*3926C>T (RAB3GAP1) ENSP00000510746.1:n.*3926C>T
ENST00000691339.1:c.*3892C>T (RAB3GAP1) ENSP00000509953.1:n.*3892C>T
ENST00000691478.1:c.*4347C>T (RAB3GAP1) ENSP00000509081.1:n.*4347C>T
ENST00000692993.1:n.1827C>T (RAB3GAP1)
ENST00000693554.1:c.*2071C>T (RAB3GAP1) ENSP00000509030.1:n.*2071C>T
ENST00000264158.13:c.*1302C>T (RAB3GAP1) MANE Select ENSP00000264158.8:n.*1302C>T
ENST00000264158.12:c.*1302C>T (RAB3GAP1) ENSP00000264158.7:n.*1302C>T
ENST00000412849.5:n.1782-4929G>A (ZRANB3)
ENST00000487003.5:n.3098+235C>T (RAB3GAP1)
ENST00000539493.2:c.2897+235C>T (RAB3GAP1) ENSP00000444306.1:n.2897+235C>T
ENST00000619650.4:c.1618-4929G>A (ZRANB3) ENSP00000480120.1:n.1618-4929G>A
NM_001172435.1:c.*1302C>T (RAB3GAP1) NP_001165906.1:n.*1302C>T
NM_012233.2:c.*1302C>T (RAB3GAP1) NP_036365.1:n.*1302C>T
XM_011510822.1:c.2935+1334C>T (RAB3GAP1) XP_011509124.1:n.2935+1334C>T
XM_011510823.1:c.2914+1334C>T (RAB3GAP1) XP_011509125.1:n.2914+1334C>T
XM_011510824.1:c.*324C>T (RAB3GAP1) XP_011509126.1:n.*324C>T
XM_011510825.1:c.*324C>T (RAB3GAP1) XP_011509127.1:n.*324C>T
XM_011510823.3:c.2914+1334C>T (RAB3GAP1) XP_011509125.1:n.2914+1334C>T
XM_011510825.3:c.*324C>T (RAB3GAP1) XP_011509127.1:n.*324C>T
XM_011511966.3:c.3049-4929G>A (ZRANB3) XP_011510268.2:n.3049-4929G>A
XR_001738674.2:n.2941+1334C>T (RAB3GAP1)
NM_001172435.2:c.*1302C>T (RAB3GAP1) NP_001165906.1:n.*1302C>T
NM_012233.3:c.*1302C>T (RAB3GAP1) MANE Select NP_036365.1:n.*1302C>T