Canonical Allele Identifier: CA1151757

Gene: RIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155900402C>T , CM000663.2:g.155900402C>T	GRCh38
NC_000001.10:g.155870193C>T , CM000663.1:g.155870193C>T	GRCh37
NC_000001.9:g.154136817C>T	NCBI36
NG_033885.1:g.16001G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006912.6:c.646G>A MANE Select	NP_008843.1:p.Asp216Asn
ENST00000368323.8:c.646G>A MANE Select	ENSP00000357306.3:p.Asp216Asn
NM_001256820.1:c.538G>A	NP_001243749.1:p.Asp180Asn
NM_001256820.2:c.538G>A	NP_001243749.1:p.Asp180Asn
NM_001256821.1:c.697G>A	NP_001243750.1:p.Asp233Asn
NM_001256821.2:c.697G>A	NP_001243750.1:p.Asp233Asn
NM_006912.5:c.646G>A	NP_008843.1:p.Asp216Asn
ENST00000368322.7:c.697G>A	ENSP00000357305.3:p.Asp233Asn
ENST00000368323.7:c.646G>A	ENSP00000357306.3:p.Asp216Asn
ENST00000461050.5:c.*375G>A	ENSP00000476319.1:n.*375G>A
ENST00000461050.6:c.*375G>A	ENSP00000476319.1:n.*375G>A
ENST00000539040.5:c.538G>A	ENSP00000441950.1:p.Asp180Asn
ENST00000539040.6:c.538G>A	ENSP00000441950.1:p.Asp180Asn
ENST00000651853.1:c.649G>A	ENSP00000498685.1:p.Asp217Asn
ENST00000704061.1:c.*317G>A	ENSP00000515664.1:n.*317G>A