Canonical Allele Identifier: CA1763383788
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10611032_10611033delinsTG , CM000670.2:g.10611032_10611033delinsTG GRCh38
NC_000008.10:g.10468542_10468543delinsTG , CM000670.1:g.10468542_10468543delinsTG GRCh37
NC_000008.9:g.10505952_10505953delinsTG NCBI36
NG_028035.1:g.49075_49076delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.3065_3066delinsCA MANE Select ENSP00000371923.3:p.Pro1022=
ENST00000382483.3:c.3065_3066delinsCA ENSP00000371923.3:p.Pro1022=
NM_178857.5:c.3065_3066delinsCA NP_849188.4:p.Pro1022=
NM_178857.6:c.3065_3066delinsCA MANE Select NP_849188.4:p.Pro1022=