Canonical Allele Identifier: CA1763389751
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622744C= , CM000670.2:g.10622744C= GRCh38
NC_000008.10:g.10480254C= , CM000670.1:g.10480254C= GRCh37
NC_000008.9:g.10517664C= NCBI36
NG_028035.1:g.37364G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.458G= MANE Select ENSP00000371923.3:p.Arg153=
ENST00000329335.3:n.708G=
ENST00000382483.3:c.458G= ENSP00000371923.3:p.Arg153=
NM_178857.5:c.458G= NP_849188.4:p.Arg153=
NM_178857.6:c.458G= MANE Select NP_849188.4:p.Arg153=