Canonical Allele Identifier: CA390994767
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882720A>T , CM000676.2:g.100882720A>T GRCh38
NC_000014.8:g.101349057A>T , CM000676.1:g.101349057A>T GRCh37
NC_000014.7:g.100418810A>T NCBI36
NG_045001.1:g.7128T>A
NG_045000.5:g.51452A>T
NG_045000.6:g.51452A>T
NG_045001.2:g.26003T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2069T>A MANE Select ENSP00000497482.1:p.Phe690Tyr
ENST00000534062.1:c.2069T>A ENSP00000435342.1:p.Phe690Tyr
NM_001134888.2:c.2069T>A NP_001128360.1:p.Phe690Tyr
NM_001134888.3:c.2069T>A MANE Select NP_001128360.1:p.Phe690Tyr