Canonical Allele Identifier: CA9516071

Gene: RTN2 PPM1N

Linked Data

• ClinVar Variation Id: 240192
• ClinVar RCV Id: RCV000230188 ; RCV000382667 ; RCV000600441 ; RCV001847960 ; RCV003311724
• dbSNP Id: rs45532933
• ExAC: 19:45992702 C / T
• gnomAD v2: 19-45992702-C-T
• gnomAD v3: 19-45489444-C-T
• gnomAD v4: 19-45489444-C-T
• MyVariant Identifiers: chr19:g.45992702C>T (hg19) ; chr19:g.45489444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489444C>T , CM000681.2:g.45489444C>T	GRCh38
NC_000019.9:g.45992702C>T , CM000681.1:g.45992702C>T	GRCh37
NC_000019.8:g.50684542C>T	NCBI36
NG_032157.1:g.12610G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1143G>A (RTN2) MANE Select	ENSP00000245923.3:p.Ala381=
ENST00000245923.8:c.1143G>A (RTN2)	ENSP00000245923.3:p.Ala381=
ENST00000344680.8:c.924G>A (RTN2)	ENSP00000345127.3:p.Ala308=
ENST00000401705.5:c.-16+465C>T (PPM1N)	ENSP00000384318.1:n.-16+465C>T
ENST00000430715.6:c.123G>A (RTN2)	ENSP00000398178.1:p.Ala41=
ENST00000587597.5:c.1143G>A (RTN2)	ENSP00000468144.1:p.Ala381=
ENST00000588036.5:n.80-458G>A (RTN2)
ENST00000589628.1:n.110G>A (RTN2)
ENST00000590526.5:c.321G>A (RTN2)	ENSP00000466619.1:p.Ala107=
ENST00000590746.5:n.62-3331G>A (RTN2)
ENST00000591286.5:c.*141G>A (RTN2)	ENSP00000467863.1:n.*141G>A
NM_005619.4:c.1143G>A (RTN2)	NP_005610.1:p.Ala381=
NM_206900.2:c.924G>A (RTN2)	NP_996783.1:p.Ala308=
NM_206901.2:c.123G>A (RTN2)	NP_996784.1:p.Ala41=
NM_005619.5:c.1143G>A (RTN2) MANE Select	NP_005610.1:p.Ala381=
NM_206900.3:c.924G>A (RTN2)	NP_996783.1:p.Ala308=
NM_206901.3:c.123G>A (RTN2)	NP_996784.1:p.Ala41=