Canonical Allele Identifier: CA1763389478
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622609G= , CM000670.2:g.10622609G= GRCh38
NC_000008.10:g.10480119G= , CM000670.1:g.10480119G= GRCh37
NC_000008.9:g.10517529G= NCBI36
NG_028035.1:g.37499C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.593C= MANE Select ENSP00000371923.3:p.Thr198=
ENST00000329335.3:n.843C=
ENST00000382483.3:c.593C= ENSP00000371923.3:p.Thr198=
NM_178857.5:c.593C= NP_849188.4:p.Thr198=
NM_178857.6:c.593C= MANE Select NP_849188.4:p.Thr198=