Canonical Allele Identifier: CA4625708
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1912320
ClinVar RCV Id: RCV002578810
dbSNP Id: rs374879431
ExAC: 8:10480288 A / C
gnomAD v2: 8-10480288-A-C
MyVariant Identifiers: chr8:g.10480288A>C (hg19) chr8:g.10622778A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622778A>C , CM000670.2:g.10622778A>C GRCh38
NC_000008.10:g.10480288A>C , CM000670.1:g.10480288A>C GRCh37
NC_000008.9:g.10517698A>C NCBI36
NG_028035.1:g.37330T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.424T>G MANE Select ENSP00000371923.3:p.Ser142Ala
ENST00000329335.3:n.674T>G
ENST00000382483.3:c.424T>G ENSP00000371923.3:p.Ser142Ala
NM_178857.5:c.424T>G NP_849188.4:p.Ser142Ala
NM_178857.6:c.424T>G MANE Select NP_849188.4:p.Ser142Ala
Search 100 bp 5'
Search 100 bp 3'