Canonical Allele Identifier: CA342802286

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874160G>C (hg19) ; chr1:g.155904369G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904369G>C , CM000663.2:g.155904369G>C	GRCh38
NC_000001.10:g.155874160G>C , CM000663.1:g.155874160G>C	GRCh37
NC_000001.9:g.154140784G>C	NCBI36
NG_033885.1:g.12034C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*100C>G	ENSP00000476319.1:n.*100C>G
ENST00000539040.6:c.263C>G	ENSP00000441950.1:p.Thr88Ser
ENST00000704061.1:c.*42C>G	ENSP00000515664.1:n.*42C>G
ENST00000368323.8:c.371C>G MANE Select	ENSP00000357306.3:p.Thr124Ser
ENST00000651853.1:c.374C>G	ENSP00000498685.1:p.Thr125Ser
ENST00000368322.7:c.422C>G	ENSP00000357305.3:p.Thr141Ser
ENST00000368323.7:c.371C>G	ENSP00000357306.3:p.Thr124Ser
ENST00000461050.5:c.*100C>G	ENSP00000476319.1:n.*100C>G
ENST00000539040.5:c.263C>G	ENSP00000441950.1:p.Thr88Ser
ENST00000609492.1:c.371C>G	ENSP00000476612.1:p.Thr124Ser
NM_001256820.1:c.263C>G	NP_001243749.1:p.Thr88Ser
NM_001256821.1:c.422C>G	NP_001243750.1:p.Thr141Ser
NM_006912.5:c.371C>G	NP_008843.1:p.Thr124Ser
NM_001256820.2:c.263C>G	NP_001243749.1:p.Thr88Ser
NM_001256821.2:c.422C>G	NP_001243750.1:p.Thr141Ser
NM_006912.6:c.371C>G MANE Select	NP_008843.1:p.Thr124Ser