Canonical Allele Identifier: CA390996042
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883290A>T , CM000676.2:g.100883290A>T GRCh38
NC_000014.8:g.101349627A>T , CM000676.1:g.101349627A>T GRCh37
NC_000014.7:g.100419380A>T NCBI36
NG_045001.1:g.6558T>A
NG_045000.5:g.52022A>T
NG_045000.6:g.52022A>T
NG_045001.2:g.25433T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1499T>A MANE Select ENSP00000497482.1:p.Phe500Tyr
ENST00000534062.1:c.1499T>A ENSP00000435342.1:p.Phe500Tyr
NM_001134888.2:c.1499T>A NP_001128360.1:p.Phe500Tyr
NM_001134888.3:c.1499T>A MANE Select NP_001128360.1:p.Phe500Tyr