Canonical Allele Identifier: CA1763379001
Gene: RP1L1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612776C= , CM000670.2:g.10612776C= GRCh38
NC_000008.10:g.10470286C= , CM000670.1:g.10470286C= GRCh37
NC_000008.9:g.10507696C= NCBI36
NG_028035.1:g.47332G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1322G= MANE Select ENSP00000371923.3:p.Gly441=
ENST00000382483.3:c.1322G= ENSP00000371923.3:p.Gly441=
NM_178857.5:c.1322G= NP_849188.4:p.Gly441=
NM_178857.6:c.1322G= MANE Select NP_849188.4:p.Gly441=
Search 100 bp 5'
Search 100 bp 3'