Canonical Allele Identifier: CA2839303932

Gene: RTN2 PPM1N

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489392del , CM000681.2:g.45489392del	GRCh38
NC_000019.9:g.45992650del , CM000681.1:g.45992650del	GRCh37
NC_000019.8:g.50684490del	NCBI36
NG_032157.1:g.12664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.1197del (RTN2) MANE Select	ENSP00000245923.3:p.Val400CysfsTer24
ENST00000245923.8:c.1197del (RTN2)	ENSP00000245923.3:p.Val400CysfsTer24
ENST00000344680.8:c.978del (RTN2)	ENSP00000345127.3:p.Val327CysfsTer24
ENST00000401705.5:c.-16+413del (PPM1N)	ENSP00000384318.1:n.-16+413del
ENST00000430715.6:c.177del (RTN2)	ENSP00000398178.1:p.Val60CysfsTer24
ENST00000587597.5:c.1197del (RTN2)	ENSP00000468144.1:p.Val400CysfsTer24
ENST00000588036.5:n.80-404del (RTN2)
ENST00000589628.1:n.164del (RTN2)
ENST00000590526.5:c.375del (RTN2)	ENSP00000466619.1:p.Val126CysfsTer24
ENST00000590746.5:n.62-3277del (RTN2)
ENST00000591286.5:c.*195del (RTN2)	ENSP00000467863.1:n.*195del
NM_005619.4:c.1197del (RTN2)	NP_005610.1:p.Val400CysfsTer24
NM_206900.2:c.978del (RTN2)	NP_996783.1:p.Val327CysfsTer24
NM_206901.2:c.177del (RTN2)	NP_996784.1:p.Val60CysfsTer24
NM_005619.5:c.1197del (RTN2) MANE Select	NP_005610.1:p.Val400CysfsTer24
NM_206900.3:c.978del (RTN2)	NP_996783.1:p.Val327CysfsTer24
NM_206901.3:c.177del (RTN2)	NP_996784.1:p.Val60CysfsTer24