Canonical Allele Identifier: CA14572719

Gene: RIT2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.43011119G>A , CM000680.2:g.43011119G>A	GRCh38
NC_000018.9:g.40591084G>A , CM000680.1:g.40591084G>A	GRCh37
NC_000018.8:g.38845082G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326695.10:c.160+22692C>T MANE Select	ENSP00000321805.4:n.160+22692C>T
ENST00000650392.1:c.160+22692C>T	ENSP00000497708.1:n.160+22692C>T
ENST00000326695.9:c.160+22692C>T	ENSP00000321805.4:n.160+22692C>T
ENST00000589109.5:c.160+22692C>T	ENSP00000467217.1:n.160+22692C>T
ENST00000590910.1:c.160+22692C>T	ENSP00000466620.1:n.160+22692C>T
NM_001272077.1:c.160+22692C>T	NP_001259006.1:n.160+22692C>T
NM_002930.3:c.160+22692C>T	NP_002921.1:n.160+22692C>T
NM_002930.4:c.160+22692C>T MANE Select	NP_002921.1:n.160+22692C>T
NM_001272077.2:c.160+22692C>T	NP_001259006.1:n.160+22692C>T