Canonical Allele Identifier: CA2159074435
Gene: RTL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882727C= , CM000676.2:g.100882727C= GRCh38
NC_000014.8:g.101349064C= , CM000676.1:g.101349064C= GRCh37
NC_000014.7:g.100418817C= NCBI36
NG_045001.1:g.7121G=
NG_045000.5:g.51459C=
NG_045000.6:g.51459C=
NG_045001.2:g.25996G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2062G= MANE Select ENSP00000497482.1:p.Ala688=
ENST00000534062.1:c.2062G= ENSP00000435342.1:p.Ala688=
NM_001134888.2:c.2062G= NP_001128360.1:p.Ala688=
NM_001134888.3:c.2062G= MANE Select NP_001128360.1:p.Ala688=