Canonical Allele Identifier: CA421058927

Gene: RIT1

Linked Data

• MyVariant Identifiers: chr1:g.155874192C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904401C>T , CM000663.2:g.155904401C>T	GRCh38
NC_000001.10:g.155874192C>T , CM000663.1:g.155874192C>T	GRCh37
NC_000001.9:g.154140816C>T	NCBI36
NG_033885.1:g.12002G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*68G>A	ENSP00000476319.1:n.*68G>A
ENST00000539040.6:c.231G>A	ENSP00000441950.1:p.Glu77=
ENST00000704061.1:c.*10G>A	ENSP00000515664.1:n.*10G>A
ENST00000368323.8:c.339G>A MANE Select	ENSP00000357306.3:p.Glu113=
ENST00000651833.1:c.339G>A	ENSP00000498732.1:p.Glu113=
ENST00000651853.1:c.342G>A	ENSP00000498685.1:p.Glu114=
ENST00000368322.7:c.390G>A	ENSP00000357305.3:p.Glu130=
ENST00000368323.7:c.339G>A	ENSP00000357306.3:p.Glu113=
ENST00000461050.5:c.*68G>A	ENSP00000476319.1:n.*68G>A
ENST00000539040.5:c.231G>A	ENSP00000441950.1:p.Glu77=
ENST00000609492.1:c.339G>A	ENSP00000476612.1:p.Glu113=
NM_001256820.1:c.231G>A	NP_001243749.1:p.Glu77=
NM_001256821.1:c.390G>A	NP_001243750.1:p.Glu130=
NM_006912.5:c.339G>A	NP_008843.1:p.Glu113=
NM_001256820.2:c.231G>A	NP_001243749.1:p.Glu77=
NM_001256821.2:c.390G>A	NP_001243750.1:p.Glu130=
NM_006912.6:c.339G>A MANE Select	NP_008843.1:p.Glu113=