Canonical Allele Identifier: CA2042193907
Gene: RASSF3 HGNC NCBI
MIR548C HGNC NCBI
MIR548Z HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64622520A= , CM000674.2:g.64622520A= GRCh38
NC_000012.11:g.65016300A= , CM000674.1:g.65016300A= GRCh37
NC_000012.10:g.63302567A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_178169.4:c.111+11777A= (RASSF3) MANE Select NP_835463.1:n.111+11777A=
ENST00000542104.6:c.111+11777A= (RASSF3) MANE Select ENSP00000443021.1:n.111+11777A=
NM_178169.3:c.111+11777A= (RASSF3) NP_835463.1:n.111+11777A=
NR_030347.1:n.12A= (MIR548C)
NR_037515.1:n.86T= (MIR548Z)
NR_040718.1:n.231+11777A= (RASSF3)
NR_040718.2:n.249+11777A= (RASSF3)
ENST00000283172.8:c.111+11777A= (RASSF3) ENSP00000283172.4:n.111+11777A=
ENST00000336061.2:c.111+11777A= (RASSF3) ENSP00000336616.2:n.111+11777A=
ENST00000542104.5:c.111+11777A= (RASSF3) ENSP00000443021.1:n.111+11777A=
ENST00000637125.1:c.295-62267A= (RASSF3) ENSP00000490100.1:n.295-62267A=
XM_011538195.1:c.75+11599A= (RASSF3) XP_011536497.1:n.75+11599A=
XM_011538195.2:c.75+11599A= (RASSF3) XP_011536497.1:n.75+11599A=