Canonical Allele Identifier: CA370300540
Gene: RP1L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622890G>C , CM000670.2:g.10622890G>C GRCh38
NC_000008.10:g.10480400G>C , CM000670.1:g.10480400G>C GRCh37
NC_000008.9:g.10517810G>C NCBI36
NG_028035.1:g.37218C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.312C>G MANE Select ENSP00000371923.3:p.Cys104Trp
ENST00000329335.3:n.562C>G
ENST00000382483.3:c.312C>G ENSP00000371923.3:p.Cys104Trp
NM_178857.5:c.312C>G NP_849188.4:p.Cys104Trp
NM_178857.6:c.312C>G MANE Select NP_849188.4:p.Cys104Trp