Canonical Allele Identifier: CA488181642

Linked Data

MyVariant Identifiers: chr14:g.101349347A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883010A>C , CM000676.2:g.100883010A>C GRCh38
NC_000014.8:g.101349347A>C , CM000676.1:g.101349347A>C GRCh37
NC_000014.7:g.100419100A>C NCBI36
NG_045001.1:g.6838T>G
NG_045000.5:g.51742A>C
NG_045000.6:g.51742A>C
NG_045001.2:g.25713T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1779T>G (RTL1) MANE Select ENSP00000497482.1:p.Ser593=
ENST00000534062.1:c.1779T>G (RTL1) ENSP00000435342.1:p.Ser593=
NM_001134888.2:c.1779T>G (RTL1) NP_001128360.1:p.Ser593=
NR_029696.1:n.32A>C (MIR127)
NM_001134888.3:c.1779T>G (RTL1) MANE Select NP_001128360.1:p.Ser593=