Canonical Allele Identifier: CA370299738
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3028060
ClinVar RCV Id: RCV003889430
gnomAD v4: 8-10622619-G-A
MyVariant Identifiers: chr8:g.10480129G>A (hg19) chr8:g.10622619G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622619G>A , CM000670.2:g.10622619G>A GRCh38
NC_000008.10:g.10480129G>A , CM000670.1:g.10480129G>A GRCh37
NC_000008.9:g.10517539G>A NCBI36
NG_028035.1:g.37489C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.583C>T MANE Select ENSP00000371923.3:p.Gln195Ter
ENST00000329335.3:n.833C>T
ENST00000382483.3:c.583C>T ENSP00000371923.3:p.Gln195Ter
NM_178857.5:c.583C>T NP_849188.4:p.Gln195Ter
NM_178857.6:c.583C>T MANE Select NP_849188.4:p.Gln195Ter
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Search 100 bp 3'