Canonical Allele Identifier: CA342802380

Gene: RIT1

Linked Data

• gnomAD v4: 1-155904394-G-A
• MyVariant Identifiers: chr1:g.155874185G>A (hg19) ; chr1:g.155904394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155904394G>A , CM000663.2:g.155904394G>A	GRCh38
NC_000001.10:g.155874185G>A , CM000663.1:g.155874185G>A	GRCh37
NC_000001.9:g.154140809G>A	NCBI36
NG_033885.1:g.12009C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461050.6:c.*75C>T	ENSP00000476319.1:n.*75C>T
ENST00000539040.6:c.238C>T	ENSP00000441950.1:p.Gln80Ter
ENST00000704061.1:c.*17C>T	ENSP00000515664.1:n.*17C>T
ENST00000368323.8:c.346C>T MANE Select	ENSP00000357306.3:p.Gln116Ter
ENST00000651833.1:c.346C>T	ENSP00000498732.1:p.Gln116Ter
ENST00000651853.1:c.349C>T	ENSP00000498685.1:p.Gln117Ter
ENST00000368322.7:c.397C>T	ENSP00000357305.3:p.Gln133Ter
ENST00000368323.7:c.346C>T	ENSP00000357306.3:p.Gln116Ter
ENST00000461050.5:c.*75C>T	ENSP00000476319.1:n.*75C>T
ENST00000539040.5:c.238C>T	ENSP00000441950.1:p.Gln80Ter
ENST00000609492.1:c.346C>T	ENSP00000476612.1:p.Gln116Ter
NM_001256820.1:c.238C>T	NP_001243749.1:p.Gln80Ter
NM_001256821.1:c.397C>T	NP_001243750.1:p.Gln133Ter
NM_006912.5:c.346C>T	NP_008843.1:p.Gln116Ter
NM_001256820.2:c.238C>T	NP_001243749.1:p.Gln80Ter
NM_001256821.2:c.397C>T	NP_001243750.1:p.Gln133Ter
NM_006912.6:c.346C>T MANE Select	NP_008843.1:p.Gln116Ter