Canonical Allele Identifier: CA1763389878

Gene: RP1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10622800G= , CM000670.2:g.10622800G=	GRCh38
NC_000008.10:g.10480310G= , CM000670.1:g.10480310G=	GRCh37
NC_000008.9:g.10517720G=	NCBI36
NG_028035.1:g.37308C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382483.4:c.402C= MANE Select	ENSP00000371923.3:p.Gly134=
ENST00000329335.3:n.652C=
ENST00000382483.3:c.402C=	ENSP00000371923.3:p.Gly134=
NM_178857.5:c.402C=	NP_849188.4:p.Gly134=
NM_178857.6:c.402C= MANE Select	NP_849188.4:p.Gly134=