Canonical Allele Identifier: CA370295784
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs756134481
gnomAD v4: 8-10612800-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612800C>A , CM000670.2:g.10612800C>A GRCh38
NC_000008.10:g.10470310C>A , CM000670.1:g.10470310C>A GRCh37
NC_000008.9:g.10507720C>A NCBI36
NG_028035.1:g.47308G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1298G>T MANE Select ENSP00000371923.3:p.Arg433Leu
ENST00000382483.3:c.1298G>T ENSP00000371923.3:p.Arg433Leu
NM_178857.5:c.1298G>T NP_849188.4:p.Arg433Leu
NM_178857.6:c.1298G>T MANE Select NP_849188.4:p.Arg433Leu