Canonical Allele Identifier: CA390994691
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2101C>T MANE Select ENSP00000497482.1:p.Gln701Ter
ENST00000534062.1:c.2101C>T ENSP00000435342.1:p.Gln701Ter
NM_001134888.2:c.2101C>T NP_001128360.1:p.Gln701Ter
NM_001134888.3:c.2101C>T MANE Select NP_001128360.1:p.Gln701Ter