Canonical Allele Identifier: CA1763389873

Gene: RP1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10622797C= , CM000670.2:g.10622797C=	GRCh38
NC_000008.10:g.10480307C= , CM000670.1:g.10480307C=	GRCh37
NC_000008.9:g.10517717C=	NCBI36
NG_028035.1:g.37311G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382483.4:c.405G= MANE Select	ENSP00000371923.3:p.Gln135=
ENST00000329335.3:n.655G=
ENST00000382483.3:c.405G=	ENSP00000371923.3:p.Gln135=
NM_178857.5:c.405G=	NP_849188.4:p.Gln135=
NM_178857.6:c.405G= MANE Select	NP_849188.4:p.Gln135=