Canonical Allele Identifier: CA390995449

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883018C>A , CM000676.2:g.100883018C>A GRCh38
NC_000014.8:g.101349355C>A , CM000676.1:g.101349355C>A GRCh37
NC_000014.7:g.100419108C>A NCBI36
NG_045001.1:g.6830G>T
NG_045000.5:g.51750C>A
NG_045000.6:g.51750C>A
NG_045001.2:g.25705G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000649591.1:c.1771G>T (RTL1) MANE Select ENSP00000497482.1:p.Glu591Ter
ENST00000534062.1:c.1771G>T (RTL1) ENSP00000435342.1:p.Glu591Ter
NM_001134888.2:c.1771G>T (RTL1) NP_001128360.1:p.Glu591Ter
NR_029696.1:n.40C>A (MIR127)
NM_001134888.3:c.1771G>T (RTL1) MANE Select NP_001128360.1:p.Glu591Ter