Canonical Allele Identifier: CA390996629
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883552G>A , CM000676.2:g.100883552G>A GRCh38
NC_000014.8:g.101349889G>A , CM000676.1:g.101349889G>A GRCh37
NC_000014.7:g.100419642G>A NCBI36
NG_045001.1:g.6296C>T
NG_045000.5:g.52284G>A
NG_045000.6:g.52284G>A
NG_045001.2:g.25171C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1237C>T MANE Select ENSP00000497482.1:p.Leu413Phe
ENST00000534062.1:c.1237C>T ENSP00000435342.1:p.Leu413Phe
NM_001134888.2:c.1237C>T NP_001128360.1:p.Leu413Phe
NM_001134888.3:c.1237C>T MANE Select NP_001128360.1:p.Leu413Phe