Canonical Allele Identifier: CA1763389312

Gene: RP1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10622489A= , CM000670.2:g.10622489A=	GRCh38
NC_000008.10:g.10479999A= , CM000670.1:g.10479999A=	GRCh37
NC_000008.9:g.10517409A=	NCBI36
NG_028035.1:g.37619T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382483.4:c.609+104T= MANE Select	ENSP00000371923.3:n.609+104T=
ENST00000329335.3:n.859+104T=
ENST00000382483.3:c.609+104T=	ENSP00000371923.3:n.609+104T=
NM_178857.5:c.609+104T=	NP_849188.4:n.609+104T=
NM_178857.6:c.609+104T= MANE Select	NP_849188.4:n.609+104T=