Canonical Allele Identifier: CA1763389780
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622755T= , CM000670.2:g.10622755T= GRCh38
NC_000008.10:g.10480265T= , CM000670.1:g.10480265T= GRCh37
NC_000008.9:g.10517675T= NCBI36
NG_028035.1:g.37353A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.447A= MANE Select ENSP00000371923.3:p.Lys149=
ENST00000329335.3:n.697A=
ENST00000382483.3:c.447A= ENSP00000371923.3:p.Lys149=
NM_178857.5:c.447A= NP_849188.4:p.Lys149=
NM_178857.6:c.447A= MANE Select NP_849188.4:p.Lys149=