Canonical Allele Identifier: CA1763389713
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622724T= , CM000670.2:g.10622724T= GRCh38
NC_000008.10:g.10480234T= , CM000670.1:g.10480234T= GRCh37
NC_000008.9:g.10517644T= NCBI36
NG_028035.1:g.37384A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.478A= MANE Select ENSP00000371923.3:p.Met160=
ENST00000329335.3:n.728A=
ENST00000382483.3:c.478A= ENSP00000371923.3:p.Met160=
NM_178857.5:c.478A= NP_849188.4:p.Met160=
NM_178857.6:c.478A= MANE Select NP_849188.4:p.Met160=