Canonical Allele Identifier: CA390994824
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882745T>G , CM000676.2:g.100882745T>G GRCh38
NC_000014.8:g.101349082T>G , CM000676.1:g.101349082T>G GRCh37
NC_000014.7:g.100418835T>G NCBI36
NG_045001.1:g.7103A>C
NG_045000.5:g.51477T>G
NG_045000.6:g.51477T>G
NG_045001.2:g.25978A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2044A>C MANE Select ENSP00000497482.1:p.Thr682Pro
ENST00000534062.1:c.2044A>C ENSP00000435342.1:p.Thr682Pro
NM_001134888.2:c.2044A>C NP_001128360.1:p.Thr682Pro
NM_001134888.3:c.2044A>C MANE Select NP_001128360.1:p.Thr682Pro