Canonical Allele Identifier: CA1662173978

Gene: RNF146

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.127285443T= , CM000668.2:g.127285443T=	GRCh38
NC_000006.11:g.127606588T= , CM000668.1:g.127606588T=	GRCh37
NC_000006.10:g.127648281T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368314.6:c.3-1173T= MANE Select	ENSP00000357297.1:n.3-1173T=
ENST00000309649.7:c.-129-607T=	ENSP00000309365.3:n.-129-607T=
ENST00000356799.6:c.3-607T=	ENSP00000349253.3:n.3-607T=
ENST00000368314.5:c.3-1173T=	ENSP00000357297.1:n.3-1173T=
ENST00000476956.5:c.3-607T=	ENSP00000477204.1:n.3-607T=
ENST00000477776.5:c.9-607T=	ENSP00000476867.1:n.9-607T=
ENST00000480444.1:c.9-607T=	ENSP00000476424.1:n.9-607T=
ENST00000489534.5:n.273-1173T=
ENST00000608340.5:n.464+95T=
ENST00000608991.5:c.-130+95T=	ENSP00000477168.1:n.-130+95T=
ENST00000609447.5:c.9-607T=	ENSP00000477019.1:n.9-607T=
ENST00000609944.5:c.9-607T=	ENSP00000477440.1:n.9-607T=
ENST00000610153.1:c.3-1173T=	ENSP00000476814.1:n.3-1173T=
ENST00000610162.5:c.-129-607T=	ENSP00000476888.1:n.-129-607T=
ENST00000616343.4:c.3-1173T=	ENSP00000479890.1:n.3-1173T=
NM_001242844.1:c.-129-607T=	NP_001229773.1:n.-129-607T=
NM_001242845.1:c.-129-607T=	NP_001229774.1:n.-129-607T=
NM_001242846.1:c.-130+95T=	NP_001229775.1:n.-130+95T=
NM_001242847.1:c.-129-607T=	NP_001229776.1:n.-129-607T=
NM_001242848.1:c.-129-607T=	NP_001229777.1:n.-129-607T=
NM_001242849.1:c.3-1173T=	NP_001229778.1:n.3-1173T=
NM_001242850.1:c.3-1173T=	NP_001229779.1:n.3-1173T=
NM_001242851.1:c.3-1173T=	NP_001229780.1:n.3-1173T=
NM_001242852.1:c.-129-607T=	NP_001229781.1:n.-129-607T=
NM_030963.3:c.-129-607T=	NP_112225.2:n.-129-607T=
XM_006715571.2:c.-130+95T=	XP_006715634.1:n.-130+95T=
XM_011536161.1:c.-129-607T=	XP_011534463.1:n.-129-607T=
XM_011536162.1:c.-130+95T=	XP_011534464.1:n.-130+95T=
XM_011536163.1:c.-130+95T=	XP_011534465.1:n.-130+95T=
XM_011536164.1:c.-129-607T=	XP_011534466.1:n.-129-607T=
XM_006715571.4:c.-130+95T=	XP_006715634.1:n.-130+95T=
XM_011536161.3:c.-129-607T=	XP_011534463.1:n.-129-607T=
XM_011536162.3:c.-130+95T=	XP_011534464.1:n.-130+95T=
XM_011536163.3:c.-130+95T=	XP_011534465.1:n.-130+95T=
XM_011536164.3:c.-129-607T=	XP_011534466.1:n.-129-607T=
XM_017011336.2:c.3-1173T=	XP_016866825.1:n.3-1173T=
XM_017011338.2:c.-130+95T=	XP_016866827.1:n.-130+95T=
XM_017011339.2:c.-129-607T=	XP_016866828.1:n.-129-607T=
XM_017011340.2:c.-130+95T=	XP_016866829.1:n.-130+95T=
XM_017011341.2:c.-129-607T=	XP_016866830.1:n.-129-607T=
XM_017011342.2:c.-130+95T=	XP_016866831.1:n.-130+95T=
XM_017011343.2:c.-130+95T=	XP_016866832.1:n.-130+95T=
XM_024446563.1:c.-130+95T=	XP_024302331.1:n.-130+95T=
XM_024446564.1:c.-130+95T=	XP_024302332.1:n.-130+95T=
NM_001242844.2:c.-129-607T=	NP_001229773.1:n.-129-607T=
NM_001242845.2:c.-129-607T=	NP_001229774.1:n.-129-607T=
NM_001242846.2:c.-130+95T=	NP_001229775.1:n.-130+95T=
NM_001242847.2:c.-129-607T=	NP_001229776.1:n.-129-607T=
NM_001242848.2:c.-129-607T=	NP_001229777.1:n.-129-607T=
NM_001242849.2:c.3-1173T=	NP_001229778.1:n.3-1173T=
NM_001242850.2:c.3-1173T= MANE Select	NP_001229779.1:n.3-1173T=
NM_001242852.2:c.-129-607T=	NP_001229781.1:n.-129-607T=
NM_030963.4:c.-129-607T=	NP_112225.2:n.-129-607T=