Canonical Allele Identifier: CA370295322
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612561C>G , CM000670.2:g.10612561C>G GRCh38
NC_000008.10:g.10470071C>G , CM000670.1:g.10470071C>G GRCh37
NC_000008.9:g.10507481C>G NCBI36
NG_028035.1:g.47547G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1537G>C MANE Select ENSP00000371923.3:p.Gly513Arg
ENST00000382483.3:c.1537G>C ENSP00000371923.3:p.Gly513Arg
NM_178857.5:c.1537G>C NP_849188.4:p.Gly513Arg
NM_178857.6:c.1537G>C MANE Select NP_849188.4:p.Gly513Arg