Canonical Allele Identifier: CA1779616091

Gene: RNF170

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42856341G= , CM000670.2:g.42856341G=	GRCh38
NC_000008.10:g.42711484G= , CM000670.1:g.42711484G=	GRCh37
NC_000008.9:g.42830641G=	NCBI36
NG_032868.1:g.45383C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527424.6:c.595C= MANE Select	ENSP00000434797.1:p.Arg199=
ENST00000240159.8:c.*170C=	ENSP00000240159.4:n.*170C=
ENST00000319073.5:c.*170C=	ENSP00000325969.5:n.*170C=
ENST00000319104.7:c.397-5344C=	ENSP00000326138.3:n.397-5344C=
ENST00000526349.5:c.343C=	ENSP00000435782.1:p.Arg115=
ENST00000527424.5:c.595C=	ENSP00000434797.1:p.Arg199=
ENST00000534961.5:c.595C=	ENSP00000445725.1:p.Arg199=
NM_001160223.1:c.595C=	NP_001153695.1:p.Arg199=
NM_001160224.1:c.397-5344C=	NP_001153696.1:n.397-5344C=
NM_001160225.1:c.343C=	NP_001153697.1:p.Arg115=
NM_030954.3:c.595C=	NP_112216.3:p.Arg199=
NR_027668.1:n.998C=
NR_027669.1:n.768C=
XM_006716404.1:c.595C=	XP_006716467.1:p.Arg199=
XM_006716405.1:c.445C=	XP_006716468.1:p.Arg149=
XM_006716406.2:c.343C=	XP_006716469.1:p.Arg115=
XM_011544666.1:c.595C=	XP_011542968.1:p.Arg199=
XM_006716404.2:c.595C=	XP_006716467.1:p.Arg199=
XM_006716405.3:c.445C=	XP_006716468.1:p.Arg149=
XM_011544666.3:c.595C=	XP_011542968.1:p.Arg199=
XM_017013881.1:c.595C=	XP_016869370.1:p.Arg199=
XM_017013882.2:c.343C=	XP_016869371.1:p.Arg115=
XR_001745604.2:n.919C=
XR_001745605.1:n.577C=
XR_001745606.1:n.609C=
XR_002956648.1:n.1081C=
XR_002956649.1:n.839C=
NM_030954.4:c.595C= MANE Select	NP_112216.3:p.Arg199=
NM_001160224.2:c.397-5344C=	NP_001153696.1:n.397-5344C=
NM_001160225.2:c.343C=	NP_001153697.1:p.Arg115=
NR_027668.2:n.880C=
NR_027669.2:n.650C=
NM_001160223.2:c.595C=	NP_001153695.1:p.Arg199=