Canonical Allele Identifier: CA1763378087
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10608307C= , CM000670.2:g.10608307C= GRCh38
NC_000008.10:g.10465817C= , CM000670.1:g.10465817C= GRCh37
NC_000008.9:g.10503227C= NCBI36
NG_028035.1:g.51801G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.5791G= MANE Select ENSP00000371923.3:p.Asp1931=
ENST00000382483.3:c.5791G= ENSP00000371923.3:p.Asp1931=
NM_178857.5:c.5791G= NP_849188.4:p.Asp1931=
NM_178857.6:c.5791G= MANE Select NP_849188.4:p.Asp1931=