Canonical Allele Identifier: CA421058954

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874198A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904407A>G , CM000663.2:g.155904407A>G	GRCh38
NC_000001.10:g.155874198A>G , CM000663.1:g.155874198A>G	GRCh37
NC_000001.9:g.154140822A>G	NCBI36
NG_033885.1:g.11996T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*62T>C	ENSP00000476319.1:n.*62T>C
ENST00000539040.6:c.225T>C	ENSP00000441950.1:p.Val75=
ENST00000704061.1:c.*4T>C	ENSP00000515664.1:n.*4T>C
ENST00000368323.8:c.333T>C MANE Select	ENSP00000357306.3:p.Val111=
ENST00000651833.1:c.333T>C	ENSP00000498732.1:p.Val111=
ENST00000651853.1:c.336T>C	ENSP00000498685.1:p.Val112=
ENST00000368322.7:c.384T>C	ENSP00000357305.3:p.Val128=
ENST00000368323.7:c.333T>C	ENSP00000357306.3:p.Val111=
ENST00000461050.5:c.*62T>C	ENSP00000476319.1:n.*62T>C
ENST00000539040.5:c.225T>C	ENSP00000441950.1:p.Val75=
ENST00000609492.1:c.333T>C	ENSP00000476612.1:p.Val111=
NM_001256820.1:c.225T>C	NP_001243749.1:p.Val75=
NM_001256821.1:c.384T>C	NP_001243750.1:p.Val128=
NM_006912.5:c.333T>C	NP_008843.1:p.Val111=
NM_001256820.2:c.225T>C	NP_001243749.1:p.Val75=
NM_001256821.2:c.384T>C	NP_001243750.1:p.Val128=
NM_006912.6:c.333T>C MANE Select	NP_008843.1:p.Val111=