Canonical Allele Identifier: CA845125895
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1297223587

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612904del , CM000670.2:g.10612904del GRCh38
NC_000008.10:g.10470414del , CM000670.1:g.10470414del GRCh37
NC_000008.9:g.10507824del NCBI36
NG_028035.1:g.47204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1194del MANE Select ENSP00000371923.3:p.Gln400SerfsTer?
ENST00000382483.3:c.1194del ENSP00000371923.3:p.Gln400SerfsTer?
NM_178857.5:c.1194del NP_849188.4:p.Gln400SerfsTer?
NM_178857.6:c.1194del MANE Select NP_849188.4:p.Gln400SerfsTer?