Canonical Allele Identifier: CA406357086

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992763A>T (hg19) ; chr19:g.45489505A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489505A>T , CM000681.2:g.45489505A>T	GRCh38
NC_000019.9:g.45992763A>T , CM000681.1:g.45992763A>T	GRCh37
NC_000019.8:g.50684603A>T	NCBI36
NG_032157.1:g.12549T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1082T>A (RTN2) MANE Select	ENSP00000245923.3:p.Phe361Tyr
ENST00000245923.8:c.1082T>A (RTN2)	ENSP00000245923.3:p.Phe361Tyr
ENST00000344680.8:c.863T>A (RTN2)	ENSP00000345127.3:p.Phe288Tyr
ENST00000401705.5:c.-16+526A>T (PPM1N)	ENSP00000384318.1:n.-16+526A>T
ENST00000430715.6:c.62T>A (RTN2)	ENSP00000398178.1:p.Phe21Tyr
ENST00000587597.5:c.1082T>A (RTN2)	ENSP00000468144.1:p.Phe361Tyr
ENST00000588036.5:n.80-519T>A (RTN2)
ENST00000589628.1:n.49T>A (RTN2)
ENST00000590526.5:c.260T>A (RTN2)	ENSP00000466619.1:p.Phe87Tyr
ENST00000590746.5:n.62-3392T>A (RTN2)
ENST00000591286.5:c.*80T>A (RTN2)	ENSP00000467863.1:n.*80T>A
NM_005619.4:c.1082T>A (RTN2)	NP_005610.1:p.Phe361Tyr
NM_206900.2:c.863T>A (RTN2)	NP_996783.1:p.Phe288Tyr
NM_206901.2:c.62T>A (RTN2)	NP_996784.1:p.Phe21Tyr
NM_005619.5:c.1082T>A (RTN2) MANE Select	NP_005610.1:p.Phe361Tyr
NM_206900.3:c.863T>A (RTN2)	NP_996783.1:p.Phe288Tyr
NM_206901.3:c.62T>A (RTN2)	NP_996784.1:p.Phe21Tyr