Canonical Allele Identifier: CA421058941

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874195A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904404A>G , CM000663.2:g.155904404A>G	GRCh38
NC_000001.10:g.155874195A>G , CM000663.1:g.155874195A>G	GRCh37
NC_000001.9:g.154140819A>G	NCBI36
NG_033885.1:g.11999T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*65T>C	ENSP00000476319.1:n.*65T>C
ENST00000539040.6:c.228T>C	ENSP00000441950.1:p.Arg76=
ENST00000704061.1:c.*7T>C	ENSP00000515664.1:n.*7T>C
ENST00000368323.8:c.336T>C MANE Select	ENSP00000357306.3:p.Arg112=
ENST00000651833.1:c.336T>C	ENSP00000498732.1:p.Arg112=
ENST00000651853.1:c.339T>C	ENSP00000498685.1:p.Arg113=
ENST00000368322.7:c.387T>C	ENSP00000357305.3:p.Arg129=
ENST00000368323.7:c.336T>C	ENSP00000357306.3:p.Arg112=
ENST00000461050.5:c.*65T>C	ENSP00000476319.1:n.*65T>C
ENST00000539040.5:c.228T>C	ENSP00000441950.1:p.Arg76=
ENST00000609492.1:c.336T>C	ENSP00000476612.1:p.Arg112=
NM_001256820.1:c.228T>C	NP_001243749.1:p.Arg76=
NM_001256821.1:c.387T>C	NP_001243750.1:p.Arg129=
NM_006912.5:c.336T>C	NP_008843.1:p.Arg112=
NM_001256820.2:c.228T>C	NP_001243749.1:p.Arg76=
NM_001256821.2:c.387T>C	NP_001243750.1:p.Arg129=
NM_006912.6:c.336T>C MANE Select	NP_008843.1:p.Arg112=