Canonical Allele Identifier: CA1763378098
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10608316C= , CM000670.2:g.10608316C= GRCh38
NC_000008.10:g.10465826C= , CM000670.1:g.10465826C= GRCh37
NC_000008.9:g.10503236C= NCBI36
NG_028035.1:g.51792G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.5782G= MANE Select ENSP00000371923.3:p.Glu1928=
ENST00000382483.3:c.5782G= ENSP00000371923.3:p.Glu1928=
NM_178857.5:c.5782G= NP_849188.4:p.Glu1928=
NM_178857.6:c.5782G= MANE Select NP_849188.4:p.Glu1928=