Canonical Allele Identifier: CA2338457684

Gene: RTN2 PPM1N

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489491C= , CM000681.2:g.45489491C=	GRCh38
NC_000019.9:g.45992749C= , CM000681.1:g.45992749C=	GRCh37
NC_000019.8:g.50684589C=	NCBI36
NG_032157.1:g.12563G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1096G= (RTN2) MANE Select	ENSP00000245923.3:p.Val366=
ENST00000245923.8:c.1096G= (RTN2)	ENSP00000245923.3:p.Val366=
ENST00000344680.8:c.877G= (RTN2)	ENSP00000345127.3:p.Val293=
ENST00000401705.5:c.-16+512C= (PPM1N)	ENSP00000384318.1:n.-16+512C=
ENST00000430715.6:c.76G= (RTN2)	ENSP00000398178.1:p.Val26=
ENST00000587597.5:c.1096G= (RTN2)	ENSP00000468144.1:p.Val366=
ENST00000588036.5:n.80-505G= (RTN2)
ENST00000589628.1:n.63G= (RTN2)
ENST00000590526.5:c.274G= (RTN2)	ENSP00000466619.1:p.Val92=
ENST00000590746.5:n.62-3378G= (RTN2)
ENST00000591286.5:c.*94G= (RTN2)	ENSP00000467863.1:n.*94G=
NM_005619.4:c.1096G= (RTN2)	NP_005610.1:p.Val366=
NM_206900.2:c.877G= (RTN2)	NP_996783.1:p.Val293=
NM_206901.2:c.76G= (RTN2)	NP_996784.1:p.Val26=
NM_005619.5:c.1096G= (RTN2) MANE Select	NP_005610.1:p.Val366=
NM_206900.3:c.877G= (RTN2)	NP_996783.1:p.Val293=
NM_206901.3:c.76G= (RTN2)	NP_996784.1:p.Val26=