Canonical Allele Identifier: CA370295322

Gene: RP1L1

Linked Data

• MyVariant Identifiers: chr8:g.10470071C>G (hg19) ; chr8:g.10612561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10612561C>G , CM000670.2:g.10612561C>G	GRCh38
NC_000008.10:g.10470071C>G , CM000670.1:g.10470071C>G	GRCh37
NC_000008.9:g.10507481C>G	NCBI36
NG_028035.1:g.47547G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382483.4:c.1537G>C MANE Select	ENSP00000371923.3:p.Gly513Arg
ENST00000382483.3:c.1537G>C	ENSP00000371923.3:p.Gly513Arg
NM_178857.5:c.1537G>C	NP_849188.4:p.Gly513Arg
NM_178857.6:c.1537G>C MANE Select	NP_849188.4:p.Gly513Arg