Canonical Allele Identifier: CA2779033574
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622794_10622881del , CM000670.2:g.10622794_10622881del GRCh38
NC_000008.10:g.10480304_10480391del , CM000670.1:g.10480304_10480391del GRCh37
NC_000008.9:g.10517714_10517801del NCBI36
NG_028035.1:g.37235_37322del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.329_416del MANE Select ENSP00000371923.3:p.Pro110GlnfsTer18
ENST00000329335.3:n.579_666del
ENST00000382483.3:c.329_416del ENSP00000371923.3:p.Pro110GlnfsTer18
NM_178857.5:c.329_416del NP_849188.4:p.Pro110GlnfsTer18
NM_178857.6:c.329_416del MANE Select NP_849188.4:p.Pro110GlnfsTer18