Canonical Allele Identifier: CA4625672
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs754311208
gnomAD v2: 8-10480220-G-C
gnomAD v4: 8-10622710-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622710G>C , CM000670.2:g.10622710G>C GRCh38
NC_000008.10:g.10480220G>C , CM000670.1:g.10480220G>C GRCh37
NC_000008.9:g.10517630G>C NCBI36
NG_028035.1:g.37398C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.492C>G MANE Select ENSP00000371923.3:p.Leu164=
ENST00000329335.3:n.742C>G
ENST00000382483.3:c.492C>G ENSP00000371923.3:p.Leu164=
NM_178857.5:c.492C>G NP_849188.4:p.Leu164=
NM_178857.6:c.492C>G MANE Select NP_849188.4:p.Leu164=