Canonical Allele Identifier: CA2042193221
Gene: RASSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64621464G= , CM000674.2:g.64621464G= GRCh38
NC_000012.11:g.65015244G= , CM000674.1:g.65015244G= GRCh37
NC_000012.10:g.63301511G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542104.6:c.111+10721G= MANE Select ENSP00000443021.1:n.111+10721G=
ENST00000637125.1:c.295-63323G= ENSP00000490100.1:n.295-63323G=
ENST00000283172.8:c.111+10721G= ENSP00000283172.4:n.111+10721G=
ENST00000336061.2:c.111+10721G= ENSP00000336616.2:n.111+10721G=
ENST00000542104.5:c.111+10721G= ENSP00000443021.1:n.111+10721G=
NM_178169.3:c.111+10721G= NP_835463.1:n.111+10721G=
NR_040718.1:n.231+10721G=
XM_011538195.1:c.75+10543G= XP_011536497.1:n.75+10543G=
XM_011538195.2:c.75+10543G= XP_011536497.1:n.75+10543G=
NM_178169.4:c.111+10721G= MANE Select NP_835463.1:n.111+10721G=
NR_040718.2:n.249+10721G=