Canonical Allele Identifier: CA459620023
Gene: RP1L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.10470117C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612607C>A , CM000670.2:g.10612607C>A GRCh38
NC_000008.10:g.10470117C>A , CM000670.1:g.10470117C>A GRCh37
NC_000008.9:g.10507527C>A NCBI36
NG_028035.1:g.47501G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1491G>T MANE Select ENSP00000371923.3:p.Gly497=
ENST00000382483.3:c.1491G>T ENSP00000371923.3:p.Gly497=
NM_178857.5:c.1491G>T NP_849188.4:p.Gly497=
NM_178857.6:c.1491G>T MANE Select NP_849188.4:p.Gly497=
Search 100 bp 5'
Search 100 bp 3'