Canonical Allele Identifier: CA342802295

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874164G>T (hg19) ; chr1:g.155904373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904373G>T , CM000663.2:g.155904373G>T	GRCh38
NC_000001.10:g.155874164G>T , CM000663.1:g.155874164G>T	GRCh37
NC_000001.9:g.154140788G>T	NCBI36
NG_033885.1:g.12030C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*96C>A	ENSP00000476319.1:n.*96C>A
ENST00000539040.6:c.259C>A	ENSP00000441950.1:p.Arg87Ser
ENST00000704061.1:c.*38C>A	ENSP00000515664.1:n.*38C>A
ENST00000368323.8:c.367C>A MANE Select	ENSP00000357306.3:p.Arg123Ser
ENST00000651853.1:c.370C>A	ENSP00000498685.1:p.Arg124Ser
ENST00000368322.7:c.418C>A	ENSP00000357305.3:p.Arg140Ser
ENST00000368323.7:c.367C>A	ENSP00000357306.3:p.Arg123Ser
ENST00000461050.5:c.*96C>A	ENSP00000476319.1:n.*96C>A
ENST00000539040.5:c.259C>A	ENSP00000441950.1:p.Arg87Ser
ENST00000609492.1:c.367C>A	ENSP00000476612.1:p.Arg123Ser
NM_001256820.1:c.259C>A	NP_001243749.1:p.Arg87Ser
NM_001256821.1:c.418C>A	NP_001243750.1:p.Arg140Ser
NM_006912.5:c.367C>A	NP_008843.1:p.Arg123Ser
NM_001256820.2:c.259C>A	NP_001243749.1:p.Arg87Ser
NM_001256821.2:c.418C>A	NP_001243750.1:p.Arg140Ser
NM_006912.6:c.367C>A MANE Select	NP_008843.1:p.Arg123Ser