Canonical Allele Identifier: CA2338457692

Gene: RTN2 PPM1N

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489511A= , CM000681.2:g.45489511A=	GRCh38
NC_000019.9:g.45992769A= , CM000681.1:g.45992769A=	GRCh37
NC_000019.8:g.50684609A=	NCBI36
NG_032157.1:g.12543T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1076T= (RTN2) MANE Select	ENSP00000245923.3:p.Val359=
ENST00000245923.8:c.1076T= (RTN2)	ENSP00000245923.3:p.Val359=
ENST00000344680.8:c.857T= (RTN2)	ENSP00000345127.3:p.Val286=
ENST00000401705.5:c.-16+532A= (PPM1N)	ENSP00000384318.1:n.-16+532A=
ENST00000430715.6:c.56T= (RTN2)	ENSP00000398178.1:p.Val19=
ENST00000587597.5:c.1076T= (RTN2)	ENSP00000468144.1:p.Val359=
ENST00000588036.5:n.80-525T= (RTN2)
ENST00000589628.1:n.43T= (RTN2)
ENST00000590526.5:c.254T= (RTN2)	ENSP00000466619.1:p.Val85=
ENST00000590746.5:n.62-3398T= (RTN2)
ENST00000591286.5:c.*74T= (RTN2)	ENSP00000467863.1:n.*74T=
NM_005619.4:c.1076T= (RTN2)	NP_005610.1:p.Val359=
NM_206900.2:c.857T= (RTN2)	NP_996783.1:p.Val286=
NM_206901.2:c.56T= (RTN2)	NP_996784.1:p.Val19=
NM_005619.5:c.1076T= (RTN2) MANE Select	NP_005610.1:p.Val359=
NM_206900.3:c.857T= (RTN2)	NP_996783.1:p.Val286=
NM_206901.3:c.56T= (RTN2)	NP_996784.1:p.Val19=