Canonical Allele Identifier: CA2579091974
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612867dup , CM000670.2:g.10612867dup GRCh38
NC_000008.10:g.10470377dup , CM000670.1:g.10470377dup GRCh37
NC_000008.9:g.10507787dup NCBI36
NG_028035.1:g.47244dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1234dup MANE Select ENSP00000371923.3:p.Leu412ProfsTer?
ENST00000382483.3:c.1234dup ENSP00000371923.3:p.Leu412ProfsTer?
NM_178857.5:c.1234dup NP_849188.4:p.Leu412ProfsTer?
NM_178857.6:c.1234dup MANE Select NP_849188.4:p.Leu412ProfsTer?