Canonical Allele Identifier: CA2526199564

Gene: RIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904508G>A , CM000663.2:g.155904508G>A	GRCh38
NC_000001.10:g.155874299G>A , CM000663.1:g.155874299G>A	GRCh37
NC_000001.9:g.154140923G>A	NCBI36
NG_033885.1:g.11895C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.246-6C>T	ENSP00000476319.1:n.246-6C>T
ENST00000539040.6:c.130-6C>T	ENSP00000441950.1:n.130-6C>T
ENST00000704061.1:c.215-6C>T	ENSP00000515664.1:n.215-6C>T
ENST00000368323.8:c.238-6C>T MANE Select	ENSP00000357306.3:n.238-6C>T
ENST00000651833.1:c.238-6C>T	ENSP00000498732.1:n.238-6C>T
ENST00000651853.1:c.241-6C>T	ENSP00000498685.1:n.241-6C>T
ENST00000368322.7:c.289-6C>T	ENSP00000357305.3:n.289-6C>T
ENST00000368323.7:c.238-6C>T	ENSP00000357306.3:n.238-6C>T
ENST00000461050.5:c.246-6C>T	ENSP00000476319.1:n.246-6C>T
ENST00000539040.5:c.130-6C>T	ENSP00000441950.1:n.130-6C>T
ENST00000609492.1:c.238-6C>T	ENSP00000476612.1:n.238-6C>T
NM_001256820.1:c.130-6C>T	NP_001243749.1:n.130-6C>T
NM_001256821.1:c.289-6C>T	NP_001243750.1:n.289-6C>T
NM_006912.5:c.238-6C>T	NP_008843.1:n.238-6C>T
NM_001256820.2:c.130-6C>T	NP_001243749.1:n.130-6C>T
NM_001256821.2:c.289-6C>T	NP_001243750.1:n.289-6C>T
NM_006912.6:c.238-6C>T MANE Select	NP_008843.1:n.238-6C>T