Canonical Allele Identifier: CA10928040

Gene: RIT1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155908941A>G , CM000663.2:g.155908941A>G	GRCh38
NC_000001.10:g.155878732A>G , CM000663.1:g.155878732A>G	GRCh37
NC_000001.9:g.154145356A>G	NCBI36
NG_033885.1:g.7462T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461050.6:c.163+1509T>C	ENSP00000476319.1:n.163+1509T>C
ENST00000539040.6:c.55+1509T>C	ENSP00000441950.1:n.55+1509T>C
ENST00000704061.1:c.214+1509T>C	ENSP00000515664.1:n.214+1509T>C
ENST00000368323.8:c.163+1509T>C MANE Select	ENSP00000357306.3:n.163+1509T>C
ENST00000650659.1:n.345+1509T>C
ENST00000651833.1:c.163+1509T>C	ENSP00000498732.1:n.163+1509T>C
ENST00000651853.1:c.163+1509T>C	ENSP00000498685.1:n.163+1509T>C
ENST00000368322.7:c.214+1509T>C	ENSP00000357305.3:n.214+1509T>C
ENST00000368323.7:c.163+1509T>C	ENSP00000357306.3:n.163+1509T>C
ENST00000461050.5:c.163+1509T>C	ENSP00000476319.1:n.163+1509T>C
ENST00000539040.5:c.55+1509T>C	ENSP00000441950.1:n.55+1509T>C
ENST00000609492.1:c.163+1509T>C	ENSP00000476612.1:n.163+1509T>C
NM_001256820.1:c.55+1509T>C	NP_001243749.1:n.55+1509T>C
NM_001256821.1:c.214+1509T>C	NP_001243750.1:n.214+1509T>C
NM_006912.5:c.163+1509T>C	NP_008843.1:n.163+1509T>C
NM_001256820.2:c.55+1509T>C	NP_001243749.1:n.55+1509T>C
NM_001256821.2:c.214+1509T>C	NP_001243750.1:n.214+1509T>C
NM_006912.6:c.163+1509T>C MANE Select	NP_008843.1:n.163+1509T>C