Canonical Allele Identifier: CA15729183

Gene: RASSF3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64618200G>A , CM000674.2:g.64618200G>A	GRCh38
NC_000012.11:g.65011980G>A , CM000674.1:g.65011980G>A	GRCh37
NC_000012.10:g.63298247G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542104.6:c.111+7457G>A MANE Select	ENSP00000443021.1:n.111+7457G>A
ENST00000637125.1:c.295-66587G>A	ENSP00000490100.1:n.295-66587G>A
ENST00000283172.8:c.111+7457G>A	ENSP00000283172.4:n.111+7457G>A
ENST00000336061.2:c.111+7457G>A	ENSP00000336616.2:n.111+7457G>A
ENST00000542104.5:c.111+7457G>A	ENSP00000443021.1:n.111+7457G>A
NM_178169.3:c.111+7457G>A	NP_835463.1:n.111+7457G>A
NR_040718.1:n.231+7457G>A
XM_011538195.1:c.75+7279G>A	XP_011536497.1:n.75+7279G>A
XM_011538195.2:c.75+7279G>A	XP_011536497.1:n.75+7279G>A
NM_178169.4:c.111+7457G>A MANE Select	NP_835463.1:n.111+7457G>A
NR_040718.2:n.249+7457G>A