Canonical Allele Identifier: CA370300254
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622792T>A , CM000670.2:g.10622792T>A GRCh38
NC_000008.10:g.10480302T>A , CM000670.1:g.10480302T>A GRCh37
NC_000008.9:g.10517712T>A NCBI36
NG_028035.1:g.37316A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.410A>T MANE Select ENSP00000371923.3:p.Glu137Val
ENST00000329335.3:n.660A>T
ENST00000382483.3:c.410A>T ENSP00000371923.3:p.Glu137Val
NM_178857.5:c.410A>T NP_849188.4:p.Glu137Val
NM_178857.6:c.410A>T MANE Select NP_849188.4:p.Glu137Val