Canonical Allele Identifier: CA2340043036
Gene: RASIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48730149C>T , CM000681.2:g.48730149C>T GRCh38
NC_000019.9:g.49233406C>T , CM000681.1:g.49233406C>T GRCh37
NC_000019.8:g.53925218C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000222145.9:c.1180-559G>A MANE Select ENSP00000222145.3:n.1180-559G>A
ENST00000222145.8:c.1180-559G>A ENSP00000222145.3:n.1180-559G>A
ENST00000594232.1:n.577-559G>A
ENST00000599291.1:c.415+5047G>A
ENST00000621604.4:c.1180-559G>A ENSP00000479419.1:n.1180-559G>A
NM_017805.2:c.1180-559G>A NP_060275.2:n.1180-559G>A
XM_011527053.1:c.1180-559G>A XP_011525355.1:n.1180-559G>A
XM_011527054.1:c.1180-559G>A XP_011525356.1:n.1180-559G>A
XM_011527055.1:c.1180-559G>A XP_011525357.1:n.1180-559G>A
XR_935837.1:n.1477-559G>A
XM_011527053.2:c.1483-559G>A XP_011525355.2:n.1483-559G>A
XM_017026914.1:c.1483-559G>A XP_016882403.1:n.1483-559G>A
XM_017026915.1:c.1483-559G>A XP_016882404.1:n.1483-559G>A
XM_024451566.1:c.1483-559G>A XP_024307334.1:n.1483-559G>A
XM_024451567.1:c.1483-559G>A XP_024307335.1:n.1483-559G>A
XR_001753712.1:n.1497-559G>A
NM_017805.3:c.1180-559G>A MANE Select NP_060275.2:n.1180-559G>A