Canonical Allele Identifier: CA1763378841
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612664G= , CM000670.2:g.10612664G= GRCh38
NC_000008.10:g.10470174G= , CM000670.1:g.10470174G= GRCh37
NC_000008.9:g.10507584G= NCBI36
NG_028035.1:g.47444C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.1434C= MANE Select ENSP00000371923.3:p.Asp478=
ENST00000382483.3:c.1434C= ENSP00000371923.3:p.Asp478=
NM_178857.5:c.1434C= NP_849188.4:p.Asp478=
NM_178857.6:c.1434C= MANE Select NP_849188.4:p.Asp478=