Canonical Allele Identifier: CA1763389745
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622742T= , CM000670.2:g.10622742T= GRCh38
NC_000008.10:g.10480252T= , CM000670.1:g.10480252T= GRCh37
NC_000008.9:g.10517662T= NCBI36
NG_028035.1:g.37366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.460A= MANE Select ENSP00000371923.3:p.Ile154=
ENST00000329335.3:n.710A=
ENST00000382483.3:c.460A= ENSP00000371923.3:p.Ile154=
NM_178857.5:c.460A= NP_849188.4:p.Ile154=
NM_178857.6:c.460A= MANE Select NP_849188.4:p.Ile154=