Canonical Allele Identifier: CA370299692
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622603C>A , CM000670.2:g.10622603C>A GRCh38
NC_000008.10:g.10480113C>A , CM000670.1:g.10480113C>A GRCh37
NC_000008.9:g.10517523C>A NCBI36
NG_028035.1:g.37505G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.599G>T MANE Select ENSP00000371923.3:p.Ser200Ile
ENST00000329335.3:n.849G>T
ENST00000382483.3:c.599G>T ENSP00000371923.3:p.Ser200Ile
NM_178857.5:c.599G>T NP_849188.4:p.Ser200Ile
NM_178857.6:c.599G>T MANE Select NP_849188.4:p.Ser200Ile