Canonical Allele Identifier: CA4625711
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs777388721

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622784dup , CM000670.2:g.10622784dup GRCh38
NC_000008.10:g.10480294dup , CM000670.1:g.10480294dup GRCh37
NC_000008.9:g.10517704dup NCBI36
NG_028035.1:g.37325dup

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.419dup MANE Select ENSP00000371923.3:p.Thr141HisfsTer9
ENST00000329335.3:n.669dup
ENST00000382483.3:c.419dup ENSP00000371923.3:p.Thr141HisfsTer9
NM_178857.5:c.419dup NP_849188.4:p.Thr141HisfsTer9
NM_178857.6:c.419dup MANE Select NP_849188.4:p.Thr141HisfsTer9