Canonical Allele Identifier: CA1763389314
Gene: RP1L1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622491C= , CM000670.2:g.10622491C= GRCh38
NC_000008.10:g.10480001C= , CM000670.1:g.10480001C= GRCh37
NC_000008.9:g.10517411C= NCBI36
NG_028035.1:g.37617G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+102G= MANE Select ENSP00000371923.3:n.609+102G=
ENST00000329335.3:n.859+102G=
ENST00000382483.3:c.609+102G= ENSP00000371923.3:n.609+102G=
NM_178857.5:c.609+102G= NP_849188.4:n.609+102G=
NM_178857.6:c.609+102G= MANE Select NP_849188.4:n.609+102G=
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