Canonical Allele Identifier: CA421058854

Gene: RIT1

Linked Data

• COSMIC: COSM4721846
• MyVariant Identifiers: chr1:g.155874159A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904368A>C , CM000663.2:g.155904368A>C	GRCh38
NC_000001.10:g.155874159A>C , CM000663.1:g.155874159A>C	GRCh37
NC_000001.9:g.154140783A>C	NCBI36
NG_033885.1:g.12035T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*101T>G	ENSP00000476319.1:n.*101T>G
ENST00000539040.6:c.264T>G	ENSP00000441950.1:p.Thr88=
ENST00000704061.1:c.*43T>G	ENSP00000515664.1:n.*43T>G
ENST00000368323.8:c.372T>G MANE Select	ENSP00000357306.3:p.Thr124=
ENST00000651853.1:c.375T>G	ENSP00000498685.1:p.Thr125=
ENST00000368322.7:c.423T>G	ENSP00000357305.3:p.Thr141=
ENST00000368323.7:c.372T>G	ENSP00000357306.3:p.Thr124=
ENST00000461050.5:c.*101T>G	ENSP00000476319.1:n.*101T>G
ENST00000539040.5:c.264T>G	ENSP00000441950.1:p.Thr88=
ENST00000609492.1:c.372T>G	ENSP00000476612.1:p.Thr124=
NM_001256820.1:c.264T>G	NP_001243749.1:p.Thr88=
NM_001256821.1:c.423T>G	NP_001243750.1:p.Thr141=
NM_006912.5:c.372T>G	NP_008843.1:p.Thr124=
NM_001256820.2:c.264T>G	NP_001243749.1:p.Thr88=
NM_001256821.2:c.423T>G	NP_001243750.1:p.Thr141=
NM_006912.6:c.372T>G MANE Select	NP_008843.1:p.Thr124=