Canonical Allele Identifier: CA1763389852

Gene: RP1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10622790C= , CM000670.2:g.10622790C=	GRCh38
NC_000008.10:g.10480300C= , CM000670.1:g.10480300C=	GRCh37
NC_000008.9:g.10517710C=	NCBI36
NG_028035.1:g.37318G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382483.4:c.412G= MANE Select	ENSP00000371923.3:p.Ala138=
ENST00000329335.3:n.662G=
ENST00000382483.3:c.412G=	ENSP00000371923.3:p.Ala138=
NM_178857.5:c.412G=	NP_849188.4:p.Ala138=
NM_178857.6:c.412G= MANE Select	NP_849188.4:p.Ala138=