Canonical Allele Identifier: CA390995679
Gene: RTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883118G>C , CM000676.2:g.100883118G>C GRCh38
NC_000014.8:g.101349455G>C , CM000676.1:g.101349455G>C GRCh37
NC_000014.7:g.100419208G>C NCBI36
NG_045001.1:g.6730C>G
NG_045000.5:g.51850G>C
NG_045000.6:g.51850G>C
NG_045001.2:g.25605C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649591.1:c.1671C>G MANE Select ENSP00000497482.1:p.His557Gln
ENST00000534062.1:c.1671C>G ENSP00000435342.1:p.His557Gln
NM_001134888.2:c.1671C>G NP_001128360.1:p.His557Gln
NM_001134888.3:c.1671C>G MANE Select NP_001128360.1:p.His557Gln