Canonical Allele Identifier: CA889715799

Gene: RIT1

Linked Data

• dbSNP Id: rs1486963391
• gnomAD v3: 1-155900666-TTG-T
• gnomAD v4: 1-155900666-TTG-T
• MyVariant Identifiers: chr1:g.155870458_155870459del (hg19) ; chr1:g.155900667_155900668del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155900668_155900669del , CM000663.2:g.155900668_155900669del	GRCh38
NC_000001.10:g.155870459_155870460del , CM000663.1:g.155870459_155870460del	GRCh37
NC_000001.9:g.154137083_154137084del	NCBI36
NG_033885.1:g.15735_15736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461050.6:c.*159-50_*159-49del	ENSP00000476319.1:n.*159-50_*159-49del
ENST00000539040.6:c.322-50_322-49del	ENSP00000441950.1:n.322-50_322-49del
ENST00000704061.1:c.*101-50_*101-49del	ENSP00000515664.1:n.*101-50_*101-49del
ENST00000368323.8:c.430-50_430-49del MANE Select	ENSP00000357306.3:n.430-50_430-49del
ENST00000651853.1:c.433-50_433-49del	ENSP00000498685.1:n.433-50_433-49del
ENST00000368322.7:c.481-50_481-49del	ENSP00000357305.3:n.481-50_481-49del
ENST00000368323.7:c.430-50_430-49del	ENSP00000357306.3:n.430-50_430-49del
ENST00000461050.5:c.*159-50_*159-49del	ENSP00000476319.1:n.*159-50_*159-49del
ENST00000539040.5:c.322-50_322-49del	ENSP00000441950.1:n.322-50_322-49del
ENST00000609492.1:c.430-50_430-49del	ENSP00000476612.1:n.430-50_430-49del
NM_001256820.1:c.322-50_322-49del	NP_001243749.1:n.322-50_322-49del
NM_001256821.1:c.481-50_481-49del	NP_001243750.1:n.481-50_481-49del
NM_006912.5:c.430-50_430-49del	NP_008843.1:n.430-50_430-49del
NM_001256820.2:c.322-50_322-49del	NP_001243749.1:n.322-50_322-49del
NM_001256821.2:c.481-50_481-49del	NP_001243750.1:n.481-50_481-49del
NM_006912.6:c.430-50_430-49del MANE Select	NP_008843.1:n.430-50_430-49del