Canonical Allele Identifier: CA390995456

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883021A>G , CM000676.2:g.100883021A>G GRCh38
NC_000014.8:g.101349358A>G , CM000676.1:g.101349358A>G GRCh37
NC_000014.7:g.100419111A>G NCBI36
NG_045001.1:g.6827T>C
NG_045000.5:g.51753A>G
NG_045000.6:g.51753A>G
NG_045001.2:g.25702T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649591.1:c.1768T>C (RTL1) MANE Select ENSP00000497482.1:p.Ser590Pro
ENST00000534062.1:c.1768T>C (RTL1) ENSP00000435342.1:p.Ser590Pro
NM_001134888.2:c.1768T>C (RTL1) NP_001128360.1:p.Ser590Pro
NR_029696.1:n.43A>G (MIR127)
NM_001134888.3:c.1768T>C (RTL1) MANE Select NP_001128360.1:p.Ser590Pro