Canonical Allele Identifier: CA390994689
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882688G>T , CM000676.2:g.100882688G>T GRCh38
NC_000014.8:g.101349025G>T , CM000676.1:g.101349025G>T GRCh37
NC_000014.7:g.100418778G>T NCBI36
NG_045001.1:g.7160C>A
NG_045000.5:g.51420G>T
NG_045000.6:g.51420G>T
NG_045001.2:g.26035C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2101C>A MANE Select ENSP00000497482.1:p.Gln701Lys
ENST00000534062.1:c.2101C>A ENSP00000435342.1:p.Gln701Lys
NM_001134888.2:c.2101C>A NP_001128360.1:p.Gln701Lys
NM_001134888.3:c.2101C>A MANE Select NP_001128360.1:p.Gln701Lys