Canonical Allele Identifier: CA406356855

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992720G>T (hg19) ; chr19:g.45489462G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489462G>T , CM000681.2:g.45489462G>T	GRCh38
NC_000019.9:g.45992720G>T , CM000681.1:g.45992720G>T	GRCh37
NC_000019.8:g.50684560G>T	NCBI36
NG_032157.1:g.12592C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.1125C>A (RTN2) MANE Select	ENSP00000245923.3:p.Ser375Arg
ENST00000245923.8:c.1125C>A (RTN2)	ENSP00000245923.3:p.Ser375Arg
ENST00000344680.8:c.906C>A (RTN2)	ENSP00000345127.3:p.Ser302Arg
ENST00000401705.5:c.-16+483G>T (PPM1N)	ENSP00000384318.1:n.-16+483G>T
ENST00000430715.6:c.105C>A (RTN2)	ENSP00000398178.1:p.Ser35Arg
ENST00000587597.5:c.1125C>A (RTN2)	ENSP00000468144.1:p.Ser375Arg
ENST00000588036.5:n.80-476C>A (RTN2)
ENST00000589628.1:n.92C>A (RTN2)
ENST00000590526.5:c.303C>A (RTN2)	ENSP00000466619.1:p.Ser101Arg
ENST00000590746.5:n.62-3349C>A (RTN2)
ENST00000591286.5:c.*123C>A (RTN2)	ENSP00000467863.1:n.*123C>A
NM_005619.4:c.1125C>A (RTN2)	NP_005610.1:p.Ser375Arg
NM_206900.2:c.906C>A (RTN2)	NP_996783.1:p.Ser302Arg
NM_206901.2:c.105C>A (RTN2)	NP_996784.1:p.Ser35Arg
NM_005619.5:c.1125C>A (RTN2) MANE Select	NP_005610.1:p.Ser375Arg
NM_206900.3:c.906C>A (RTN2)	NP_996783.1:p.Ser302Arg
NM_206901.3:c.105C>A (RTN2)	NP_996784.1:p.Ser35Arg