Canonical Allele Identifier: CA370300042
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622723A>T , CM000670.2:g.10622723A>T GRCh38
NC_000008.10:g.10480233A>T , CM000670.1:g.10480233A>T GRCh37
NC_000008.9:g.10517643A>T NCBI36
NG_028035.1:g.37385T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.479T>A MANE Select ENSP00000371923.3:p.Met160Lys
ENST00000329335.3:n.729T>A
ENST00000382483.3:c.479T>A ENSP00000371923.3:p.Met160Lys
NM_178857.5:c.479T>A NP_849188.4:p.Met160Lys
NM_178857.6:c.479T>A MANE Select NP_849188.4:p.Met160Lys