Canonical Allele Identifier: CA2159075062
Gene: RTL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883342G= , CM000676.2:g.100883342G= GRCh38
NC_000014.8:g.101349679G= , CM000676.1:g.101349679G= GRCh37
NC_000014.7:g.100419432G= NCBI36
NG_045001.1:g.6506C=
NG_045000.5:g.52074G=
NG_045000.6:g.52074G=
NG_045001.2:g.25381C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1447C= MANE Select ENSP00000497482.1:p.His483=
ENST00000534062.1:c.1447C= ENSP00000435342.1:p.His483=
NM_001134888.2:c.1447C= NP_001128360.1:p.His483=
NM_001134888.3:c.1447C= MANE Select NP_001128360.1:p.His483=