Canonical Allele Identifier: CA390994690
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2101C>G MANE Select ENSP00000497482.1:p.Gln701Glu
ENST00000534062.1:c.2101C>G ENSP00000435342.1:p.Gln701Glu
NM_001134888.2:c.2101C>G NP_001128360.1:p.Gln701Glu
NM_001134888.3:c.2101C>G MANE Select NP_001128360.1:p.Gln701Glu