Canonical Allele Identifier: CA1763383994
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10611139G= , CM000670.2:g.10611139G= GRCh38
NC_000008.10:g.10468649G= , CM000670.1:g.10468649G= GRCh37
NC_000008.9:g.10506059G= NCBI36
NG_028035.1:g.48969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.2959C= MANE Select ENSP00000371923.3:p.Leu987=
ENST00000382483.3:c.2959C= ENSP00000371923.3:p.Leu987=
NM_178857.5:c.2959C= NP_849188.4:p.Leu987=
NM_178857.6:c.2959C= MANE Select NP_849188.4:p.Leu987=