Canonical Allele Identifier: CA1763378713
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612564G= , CM000670.2:g.10612564G= GRCh38
NC_000008.10:g.10470074G= , CM000670.1:g.10470074G= GRCh37
NC_000008.9:g.10507484G= NCBI36
NG_028035.1:g.47544C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1534C= MANE Select ENSP00000371923.3:p.Leu512=
ENST00000382483.3:c.1534C= ENSP00000371923.3:p.Leu512=
NM_178857.5:c.1534C= NP_849188.4:p.Leu512=
NM_178857.6:c.1534C= MANE Select NP_849188.4:p.Leu512=