Canonical Allele Identifier: CA1763389213

Gene: RP1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10622468C= , CM000670.2:g.10622468C=	GRCh38
NC_000008.10:g.10479978C= , CM000670.1:g.10479978C=	GRCh37
NC_000008.9:g.10517388C=	NCBI36
NG_028035.1:g.37640G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382483.4:c.609+125G= MANE Select	ENSP00000371923.3:n.609+125G=
ENST00000329335.3:n.859+125G=
ENST00000382483.3:c.609+125G=	ENSP00000371923.3:n.609+125G=
NM_178857.5:c.609+125G=	NP_849188.4:n.609+125G=
NM_178857.6:c.609+125G= MANE Select	NP_849188.4:n.609+125G=