Canonical Allele Identifier: CA406356317

Gene: RTN2 PPM1N

Linked Data

• dbSNP Id: rs1280056583
• gnomAD v4: 19-45489394-C-T
• MyVariant Identifiers: chr19:g.45992652C>T (hg19) ; chr19:g.45489394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489394C>T , CM000681.2:g.45489394C>T	GRCh38
NC_000019.9:g.45992652C>T , CM000681.1:g.45992652C>T	GRCh37
NC_000019.8:g.50684492C>T	NCBI36
NG_032157.1:g.12660G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1193G>A (RTN2) MANE Select	ENSP00000245923.3:p.Arg398His
ENST00000245923.8:c.1193G>A (RTN2)	ENSP00000245923.3:p.Arg398His
ENST00000344680.8:c.974G>A (RTN2)	ENSP00000345127.3:p.Arg325His
ENST00000401705.5:c.-16+415C>T (PPM1N)	ENSP00000384318.1:n.-16+415C>T
ENST00000430715.6:c.173G>A (RTN2)	ENSP00000398178.1:p.Arg58His
ENST00000587597.5:c.1193G>A (RTN2)	ENSP00000468144.1:p.Arg398His
ENST00000588036.5:n.80-408G>A (RTN2)
ENST00000589628.1:n.160G>A (RTN2)
ENST00000590526.5:c.371G>A (RTN2)	ENSP00000466619.1:p.Arg124His
ENST00000590746.5:n.62-3281G>A (RTN2)
ENST00000591286.5:c.*191G>A (RTN2)	ENSP00000467863.1:n.*191G>A
NM_005619.4:c.1193G>A (RTN2)	NP_005610.1:p.Arg398His
NM_206900.2:c.974G>A (RTN2)	NP_996783.1:p.Arg325His
NM_206901.2:c.173G>A (RTN2)	NP_996784.1:p.Arg58His
NM_005619.5:c.1193G>A (RTN2) MANE Select	NP_005610.1:p.Arg398His
NM_206900.3:c.974G>A (RTN2)	NP_996783.1:p.Arg325His
NM_206901.3:c.173G>A (RTN2)	NP_996784.1:p.Arg58His