Canonical Allele Identifier: CA1763389861
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622793C= , CM000670.2:g.10622793C= GRCh38
NC_000008.10:g.10480303C= , CM000670.1:g.10480303C= GRCh37
NC_000008.9:g.10517713C= NCBI36
NG_028035.1:g.37315G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.409G= MANE Select ENSP00000371923.3:p.Glu137=
ENST00000329335.3:n.659G=
ENST00000382483.3:c.409G= ENSP00000371923.3:p.Glu137=
NM_178857.5:c.409G= NP_849188.4:p.Glu137=
NM_178857.6:c.409G= MANE Select NP_849188.4:p.Glu137=