Canonical Allele Identifier: CA1763378992
Gene: RP1L1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612771C= , CM000670.2:g.10612771C= GRCh38
NC_000008.10:g.10470281C= , CM000670.1:g.10470281C= GRCh37
NC_000008.9:g.10507691C= NCBI36
NG_028035.1:g.47337G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1327G= MANE Select ENSP00000371923.3:p.Ala443=
ENST00000382483.3:c.1327G= ENSP00000371923.3:p.Ala443=
NM_178857.5:c.1327G= NP_849188.4:p.Ala443=
NM_178857.6:c.1327G= MANE Select NP_849188.4:p.Ala443=
Search 100 bp 5'
Search 100 bp 3'