Canonical Allele Identifier: CA1763389864
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622794A= , CM000670.2:g.10622794A= GRCh38
NC_000008.10:g.10480304A= , CM000670.1:g.10480304A= GRCh37
NC_000008.9:g.10517714A= NCBI36
NG_028035.1:g.37314T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.408T= MANE Select ENSP00000371923.3:p.Arg136=
ENST00000329335.3:n.658T=
ENST00000382483.3:c.408T= ENSP00000371923.3:p.Arg136=
NM_178857.5:c.408T= NP_849188.4:p.Arg136=
NM_178857.6:c.408T= MANE Select NP_849188.4:p.Arg136=