Canonical Allele Identifier: CA390996137
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883331G>T , CM000676.2:g.100883331G>T GRCh38
NC_000014.8:g.101349668G>T , CM000676.1:g.101349668G>T GRCh37
NC_000014.7:g.100419421G>T NCBI36
NG_045001.1:g.6517C>A
NG_045000.5:g.52063G>T
NG_045000.6:g.52063G>T
NG_045001.2:g.25392C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1458C>A MANE Select ENSP00000497482.1:p.His486Gln
ENST00000534062.1:c.1458C>A ENSP00000435342.1:p.His486Gln
NM_001134888.2:c.1458C>A NP_001128360.1:p.His486Gln
NM_001134888.3:c.1458C>A MANE Select NP_001128360.1:p.His486Gln