Canonical Allele Identifier: CA3191667592
Gene: RASSF3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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