Canonical Allele Identifier: CA1763389650
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622699A= , CM000670.2:g.10622699A= GRCh38
NC_000008.10:g.10480209A= , CM000670.1:g.10480209A= GRCh37
NC_000008.9:g.10517619A= NCBI36
NG_028035.1:g.37409T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.503T= MANE Select ENSP00000371923.3:p.Val168=
ENST00000329335.3:n.753T=
ENST00000382483.3:c.503T= ENSP00000371923.3:p.Val168=
NM_178857.5:c.503T= NP_849188.4:p.Val168=
NM_178857.6:c.503T= MANE Select NP_849188.4:p.Val168=