Canonical Allele Identifier: CA1763390329
Gene: RP1L1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622949G= , CM000670.2:g.10622949G= GRCh38
NC_000008.10:g.10480459G= , CM000670.1:g.10480459G= GRCh37
NC_000008.9:g.10517869G= NCBI36
NG_028035.1:g.37159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.253C= MANE Select ENSP00000371923.3:p.Arg85=
ENST00000329335.3:n.503C=
ENST00000382483.3:c.253C= ENSP00000371923.3:p.Arg85=
NM_178857.5:c.253C= NP_849188.4:p.Arg85=
NM_178857.6:c.253C= MANE Select NP_849188.4:p.Arg85=
Search 100 bp 5'
Search 100 bp 3'