Canonical Allele Identifier: CA1763390126
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622878C= , CM000670.2:g.10622878C= GRCh38
NC_000008.10:g.10480388C= , CM000670.1:g.10480388C= GRCh37
NC_000008.9:g.10517798C= NCBI36
NG_028035.1:g.37230G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.324G= MANE Select ENSP00000371923.3:p.Lys108=
ENST00000329335.3:n.574G=
ENST00000382483.3:c.324G= ENSP00000371923.3:p.Lys108=
NM_178857.5:c.324G= NP_849188.4:p.Lys108=
NM_178857.6:c.324G= MANE Select NP_849188.4:p.Lys108=