Canonical Allele Identifier: CA2686114374
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622591dup , CM000670.2:g.10622591dup GRCh38
NC_000008.10:g.10480101dup , CM000670.1:g.10480101dup GRCh37
NC_000008.9:g.10517511dup NCBI36
NG_028035.1:g.37517dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+2dup MANE Select ENSP00000371923.3:n.609+2dup
ENST00000329335.3:n.859+2dup
ENST00000382483.3:c.609+2dup ENSP00000371923.3:n.609+2dup
NM_178857.5:c.609+2dup NP_849188.4:n.609+2dup
NM_178857.6:c.609+2dup MANE Select NP_849188.4:n.609+2dup