Canonical Allele Identifier: CA171954710
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs934595091

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622785del , CM000670.2:g.10622785del GRCh38
NC_000008.10:g.10480295del , CM000670.1:g.10480295del GRCh37
NC_000008.9:g.10517705del NCBI36
NG_028035.1:g.37323del

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.417del MANE Select ENSP00000371923.3:p.Gly140AlafsTer17
ENST00000329335.3:n.667del
ENST00000382483.3:c.417del ENSP00000371923.3:p.Gly140AlafsTer17
NM_178857.5:c.417del NP_849188.4:p.Gly140AlafsTer17
NM_178857.6:c.417del MANE Select NP_849188.4:p.Gly140AlafsTer17