Canonical Allele Identifier: CA406356850

Gene: RTN2 PPM1N

Linked Data

• dbSNP Id: rs1210595046
• gnomAD v2: 19-45992719-T-C
• gnomAD v4: 19-45489461-T-C
• MyVariant Identifiers: chr19:g.45992719T>C (hg19) ; chr19:g.45489461T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489461T>C , CM000681.2:g.45489461T>C	GRCh38
NC_000019.9:g.45992719T>C , CM000681.1:g.45992719T>C	GRCh37
NC_000019.8:g.50684559T>C	NCBI36
NG_032157.1:g.12593A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.1126A>G (RTN2) MANE Select	ENSP00000245923.3:p.Ile376Val
ENST00000245923.8:c.1126A>G (RTN2)	ENSP00000245923.3:p.Ile376Val
ENST00000344680.8:c.907A>G (RTN2)	ENSP00000345127.3:p.Ile303Val
ENST00000401705.5:c.-16+482T>C (PPM1N)	ENSP00000384318.1:n.-16+482T>C
ENST00000430715.6:c.106A>G (RTN2)	ENSP00000398178.1:p.Ile36Val
ENST00000587597.5:c.1126A>G (RTN2)	ENSP00000468144.1:p.Ile376Val
ENST00000588036.5:n.80-475A>G (RTN2)
ENST00000589628.1:n.93A>G (RTN2)
ENST00000590526.5:c.304A>G (RTN2)	ENSP00000466619.1:p.Ile102Val
ENST00000590746.5:n.62-3348A>G (RTN2)
ENST00000591286.5:c.*124A>G (RTN2)	ENSP00000467863.1:n.*124A>G
NM_005619.4:c.1126A>G (RTN2)	NP_005610.1:p.Ile376Val
NM_206900.2:c.907A>G (RTN2)	NP_996783.1:p.Ile303Val
NM_206901.2:c.106A>G (RTN2)	NP_996784.1:p.Ile36Val
NM_005619.5:c.1126A>G (RTN2) MANE Select	NP_005610.1:p.Ile376Val
NM_206900.3:c.907A>G (RTN2)	NP_996783.1:p.Ile303Val
NM_206901.3:c.106A>G (RTN2)	NP_996784.1:p.Ile36Val