Canonical Allele Identifier: CA406356324

Gene: RTN2 PPM1N

Linked Data

• gnomAD v4: 19-45489395-G-T
• MyVariant Identifiers: chr19:g.45992653G>T (hg19) ; chr19:g.45489395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489395G>T , CM000681.2:g.45489395G>T	GRCh38
NC_000019.9:g.45992653G>T , CM000681.1:g.45992653G>T	GRCh37
NC_000019.8:g.50684493G>T	NCBI36
NG_032157.1:g.12659C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1192C>A (RTN2) MANE Select	ENSP00000245923.3:p.Arg398Ser
ENST00000245923.8:c.1192C>A (RTN2)	ENSP00000245923.3:p.Arg398Ser
ENST00000344680.8:c.973C>A (RTN2)	ENSP00000345127.3:p.Arg325Ser
ENST00000401705.5:c.-16+416G>T (PPM1N)	ENSP00000384318.1:n.-16+416G>T
ENST00000430715.6:c.172C>A (RTN2)	ENSP00000398178.1:p.Arg58Ser
ENST00000587597.5:c.1192C>A (RTN2)	ENSP00000468144.1:p.Arg398Ser
ENST00000588036.5:n.80-409C>A (RTN2)
ENST00000589628.1:n.159C>A (RTN2)
ENST00000590526.5:c.370C>A (RTN2)	ENSP00000466619.1:p.Arg124Ser
ENST00000590746.5:n.62-3282C>A (RTN2)
ENST00000591286.5:c.*190C>A (RTN2)	ENSP00000467863.1:n.*190C>A
NM_005619.4:c.1192C>A (RTN2)	NP_005610.1:p.Arg398Ser
NM_206900.2:c.973C>A (RTN2)	NP_996783.1:p.Arg325Ser
NM_206901.2:c.172C>A (RTN2)	NP_996784.1:p.Arg58Ser
NM_005619.5:c.1192C>A (RTN2) MANE Select	NP_005610.1:p.Arg398Ser
NM_206900.3:c.973C>A (RTN2)	NP_996783.1:p.Arg325Ser
NM_206901.3:c.172C>A (RTN2)	NP_996784.1:p.Arg58Ser