Canonical Allele Identifier: CA1779616078

Gene: RNF170

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42856296T= , CM000670.2:g.42856296T=	GRCh38
NC_000008.10:g.42711439T= , CM000670.1:g.42711439T=	GRCh37
NC_000008.9:g.42830596T=	NCBI36
NG_032868.1:g.45428A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527424.6:c.640A= MANE Select	ENSP00000434797.1:p.Ile214=
ENST00000240159.8:c.*215A=	ENSP00000240159.4:n.*215A=
ENST00000319073.5:c.*215A=	ENSP00000325969.5:n.*215A=
ENST00000319104.7:c.397-5299A=	ENSP00000326138.3:n.397-5299A=
ENST00000526349.5:c.388A=	ENSP00000435782.1:p.Ile130=
ENST00000527424.5:c.640A=	ENSP00000434797.1:p.Ile214=
ENST00000534961.5:c.640A=	ENSP00000445725.1:p.Ile214=
NM_001160223.1:c.640A=	NP_001153695.1:p.Ile214=
NM_001160224.1:c.397-5299A=	NP_001153696.1:n.397-5299A=
NM_001160225.1:c.388A=	NP_001153697.1:p.Ile130=
NM_030954.3:c.640A=	NP_112216.3:p.Ile214=
NR_027668.1:n.1043A=
NR_027669.1:n.813A=
XM_006716404.1:c.640A=	XP_006716467.1:p.Ile214=
XM_006716405.1:c.490A=	XP_006716468.1:p.Ile164=
XM_006716406.2:c.388A=	XP_006716469.1:p.Ile130=
XM_011544666.1:c.640A=	XP_011542968.1:p.Ile214=
XM_006716404.2:c.640A=	XP_006716467.1:p.Ile214=
XM_006716405.3:c.490A=	XP_006716468.1:p.Ile164=
XM_011544666.3:c.640A=	XP_011542968.1:p.Ile214=
XM_017013881.1:c.640A=	XP_016869370.1:p.Ile214=
XM_017013882.2:c.388A=	XP_016869371.1:p.Ile130=
XR_001745604.2:n.964A=
XR_001745605.1:n.622A=
XR_001745606.1:n.654A=
XR_002956648.1:n.1126A=
XR_002956649.1:n.884A=
NM_030954.4:c.640A= MANE Select	NP_112216.3:p.Ile214=
NM_001160224.2:c.397-5299A=	NP_001153696.1:n.397-5299A=
NM_001160225.2:c.388A=	NP_001153697.1:p.Ile130=
NR_027668.2:n.925A=
NR_027669.2:n.695A=
NM_001160223.2:c.640A=	NP_001153695.1:p.Ile214=