Canonical Allele Identifier: CA1763390158
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622894A= , CM000670.2:g.10622894A= GRCh38
NC_000008.10:g.10480404A= , CM000670.1:g.10480404A= GRCh37
NC_000008.9:g.10517814A= NCBI36
NG_028035.1:g.37214T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.308T= MANE Select ENSP00000371923.3:p.Leu103=
ENST00000329335.3:n.558T=
ENST00000382483.3:c.308T= ENSP00000371923.3:p.Leu103=
NM_178857.5:c.308T= NP_849188.4:p.Leu103=
NM_178857.6:c.308T= MANE Select NP_849188.4:p.Leu103=