Canonical Allele Identifier: CA1763379009
Gene: RP1L1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612779T= , CM000670.2:g.10612779T= GRCh38
NC_000008.10:g.10470289T= , CM000670.1:g.10470289T= GRCh37
NC_000008.9:g.10507699T= NCBI36
NG_028035.1:g.47329A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1319A= MANE Select ENSP00000371923.3:p.His440=
ENST00000382483.3:c.1319A= ENSP00000371923.3:p.His440=
NM_178857.5:c.1319A= NP_849188.4:p.His440=
NM_178857.6:c.1319A= MANE Select NP_849188.4:p.His440=
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