Canonical Allele Identifier: CA1763389352
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622528T= , CM000670.2:g.10622528T= GRCh38
NC_000008.10:g.10480038T= , CM000670.1:g.10480038T= GRCh37
NC_000008.9:g.10517448T= NCBI36
NG_028035.1:g.37580A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+65A= MANE Select ENSP00000371923.3:n.609+65A=
ENST00000329335.3:n.859+65A=
ENST00000382483.3:c.609+65A= ENSP00000371923.3:n.609+65A=
NM_178857.5:c.609+65A= NP_849188.4:n.609+65A=
NM_178857.6:c.609+65A= MANE Select NP_849188.4:n.609+65A=