Canonical Allele Identifier: CA342802980

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874293C>A (hg19) ; chr1:g.155904502C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904502C>A , CM000663.2:g.155904502C>A	GRCh38
NC_000001.10:g.155874293C>A , CM000663.1:g.155874293C>A	GRCh37
NC_000001.9:g.154140917C>A	NCBI36
NG_033885.1:g.11901G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.246G>T	ENSP00000476319.1:p.Arg82Ser
ENST00000539040.6:c.130G>T	ENSP00000441950.1:p.Ala44Ser
ENST00000704061.1:c.215G>T	ENSP00000515664.1:p.Gly72Val
ENST00000368323.8:c.238G>T MANE Select	ENSP00000357306.3:p.Ala80Ser
ENST00000651833.1:c.238G>T	ENSP00000498732.1:p.Ala80Ser
ENST00000651853.1:c.241G>T	ENSP00000498685.1:p.Ala81Ser
ENST00000368322.7:c.289G>T	ENSP00000357305.3:p.Ala97Ser
ENST00000368323.7:c.238G>T	ENSP00000357306.3:p.Ala80Ser
ENST00000461050.5:c.246G>T	ENSP00000476319.1:p.Arg82Ser
ENST00000539040.5:c.130G>T	ENSP00000441950.1:p.Ala44Ser
ENST00000609492.1:c.238G>T	ENSP00000476612.1:p.Ala80Ser
NM_001256820.1:c.130G>T	NP_001243749.1:p.Ala44Ser
NM_001256821.1:c.289G>T	NP_001243750.1:p.Ala97Ser
NM_006912.5:c.238G>T	NP_008843.1:p.Ala80Ser
NM_001256820.2:c.130G>T	NP_001243749.1:p.Ala44Ser
NM_001256821.2:c.289G>T	NP_001243750.1:p.Ala97Ser
NM_006912.6:c.238G>T MANE Select	NP_008843.1:p.Ala80Ser