Canonical Allele Identifier: CA1763389640
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622692G= , CM000670.2:g.10622692G= GRCh38
NC_000008.10:g.10480202G= , CM000670.1:g.10480202G= GRCh37
NC_000008.9:g.10517612G= NCBI36
NG_028035.1:g.37416C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.510C= MANE Select ENSP00000371923.3:p.Leu170=
ENST00000329335.3:n.760C=
ENST00000382483.3:c.510C= ENSP00000371923.3:p.Leu170=
NM_178857.5:c.510C= NP_849188.4:p.Leu170=
NM_178857.6:c.510C= MANE Select NP_849188.4:p.Leu170=