Canonical Allele Identifier: CA2159075048
Gene: RTL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883295C= , CM000676.2:g.100883295C= GRCh38
NC_000014.8:g.101349632C= , CM000676.1:g.101349632C= GRCh37
NC_000014.7:g.100419385C= NCBI36
NG_045001.1:g.6553G=
NG_045000.5:g.52027C=
NG_045000.6:g.52027C=
NG_045001.2:g.25428G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1494G= MANE Select ENSP00000497482.1:p.Pro498=
ENST00000534062.1:c.1494G= ENSP00000435342.1:p.Pro498=
NM_001134888.2:c.1494G= NP_001128360.1:p.Pro498=
NM_001134888.3:c.1494G= MANE Select NP_001128360.1:p.Pro498=