Canonical Allele Identifier: CA1200375893

Gene: RIT1

Linked Data

• dbSNP Id: rs372437511

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904275T>A , CM000663.2:g.155904275T>A	GRCh38
NC_000001.10:g.155874066T>A , CM000663.1:g.155874066T>A	GRCh37
NC_000001.9:g.154140690T>A	NCBI36
NG_033885.1:g.12128A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*158+36A>T	ENSP00000476319.1:n.*158+36A>T
ENST00000539040.6:c.321+36A>T	ENSP00000441950.1:n.321+36A>T
ENST00000704061.1:c.*100+36A>T	ENSP00000515664.1:n.*100+36A>T
ENST00000368323.8:c.429+36A>T MANE Select	ENSP00000357306.3:n.429+36A>T
ENST00000651853.1:c.432+36A>T	ENSP00000498685.1:n.432+36A>T
ENST00000368322.7:c.480+36A>T	ENSP00000357305.3:n.480+36A>T
ENST00000368323.7:c.429+36A>T	ENSP00000357306.3:n.429+36A>T
ENST00000461050.5:c.*158+36A>T	ENSP00000476319.1:n.*158+36A>T
ENST00000539040.5:c.321+36A>T	ENSP00000441950.1:n.321+36A>T
ENST00000609492.1:c.429+36A>T	ENSP00000476612.1:n.429+36A>T
NM_001256820.1:c.321+36A>T	NP_001243749.1:n.321+36A>T
NM_001256821.1:c.480+36A>T	NP_001243750.1:n.480+36A>T
NM_006912.5:c.429+36A>T	NP_008843.1:n.429+36A>T
NM_001256820.2:c.321+36A>T	NP_001243749.1:n.321+36A>T
NM_001256821.2:c.480+36A>T	NP_001243750.1:n.480+36A>T
NM_006912.6:c.429+36A>T MANE Select	NP_008843.1:n.429+36A>T