Canonical Allele Identifier: CA390996607
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883542C>A , CM000676.2:g.100883542C>A GRCh38
NC_000014.8:g.101349879C>A , CM000676.1:g.101349879C>A GRCh37
NC_000014.7:g.100419632C>A NCBI36
NG_045001.1:g.6306G>T
NG_045000.5:g.52274C>A
NG_045000.6:g.52274C>A
NG_045001.2:g.25181G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1247G>T MANE Select ENSP00000497482.1:p.Arg416Ile
ENST00000534062.1:c.1247G>T ENSP00000435342.1:p.Arg416Ile
NM_001134888.2:c.1247G>T NP_001128360.1:p.Arg416Ile
NM_001134888.3:c.1247G>T MANE Select NP_001128360.1:p.Arg416Ile