Canonical Allele Identifier: CA2159074421
Gene: RTL1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2069T= MANE Select ENSP00000497482.1:p.Phe690=
ENST00000534062.1:c.2069T= ENSP00000435342.1:p.Phe690=
NM_001134888.2:c.2069T= NP_001128360.1:p.Phe690=
NM_001134888.3:c.2069T= MANE Select NP_001128360.1:p.Phe690=