Canonical Allele Identifier: CA370295782
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1797891590

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612798A>T , CM000670.2:g.10612798A>T GRCh38
NC_000008.10:g.10470308A>T , CM000670.1:g.10470308A>T GRCh37
NC_000008.9:g.10507718A>T NCBI36
NG_028035.1:g.47310T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1300T>A MANE Select ENSP00000371923.3:p.Cys434Ser
ENST00000382483.3:c.1300T>A ENSP00000371923.3:p.Cys434Ser
NM_178857.5:c.1300T>A NP_849188.4:p.Cys434Ser
NM_178857.6:c.1300T>A MANE Select NP_849188.4:p.Cys434Ser