Canonical Allele Identifier: CA2159074411
Gene: RTL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882703C= , CM000676.2:g.100882703C= GRCh38
NC_000014.8:g.101349040C= , CM000676.1:g.101349040C= GRCh37
NC_000014.7:g.100418793C= NCBI36
NG_045001.1:g.7145G=
NG_045000.5:g.51435C=
NG_045000.6:g.51435C=
NG_045001.2:g.26020G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2086G= MANE Select ENSP00000497482.1:p.Glu696=
ENST00000534062.1:c.2086G= ENSP00000435342.1:p.Glu696=
NM_001134888.2:c.2086G= NP_001128360.1:p.Glu696=
NM_001134888.3:c.2086G= MANE Select NP_001128360.1:p.Glu696=