Canonical Allele Identifier: CA4625654
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs181942944
gnomAD v2: 8-10480174-C-A
gnomAD v3: 8-10622664-C-A
gnomAD v4: 8-10622664-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622664C>A , CM000670.2:g.10622664C>A GRCh38
NC_000008.10:g.10480174C>A , CM000670.1:g.10480174C>A GRCh37
NC_000008.9:g.10517584C>A NCBI36
NG_028035.1:g.37444G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.538G>T MANE Select ENSP00000371923.3:p.Ala180Ser
ENST00000329335.3:n.788G>T
ENST00000382483.3:c.538G>T ENSP00000371923.3:p.Ala180Ser
NM_178857.5:c.538G>T NP_849188.4:p.Ala180Ser
NM_178857.6:c.538G>T MANE Select NP_849188.4:p.Ala180Ser