Canonical Allele Identifier: CA2960920485

Gene: RTN2 PPM1N

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489069A>G , CM000681.2:g.45489069A>G	GRCh38
NC_000019.9:g.45992327A>G , CM000681.1:g.45992327A>G	GRCh37
NC_000019.8:g.50684167A>G	NCBI36
NG_032157.1:g.12985T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005619.5:c.1242-83T>C (RTN2) MANE Select	NP_005610.1:n.1242-83T>C
ENST00000245923.9:c.1242-83T>C (RTN2) MANE Select	ENSP00000245923.3:n.1242-83T>C
NM_005619.4:c.1242-83T>C (RTN2)	NP_005610.1:n.1242-83T>C
NM_206900.2:c.1023-83T>C (RTN2)	NP_996783.1:n.1023-83T>C
NM_206900.3:c.1023-83T>C (RTN2)	NP_996783.1:n.1023-83T>C
NM_206901.2:c.222-83T>C (RTN2)	NP_996784.1:n.222-83T>C
NM_206901.3:c.222-83T>C (RTN2)	NP_996784.1:n.222-83T>C
ENST00000245923.8:c.1242-83T>C (RTN2)	ENSP00000245923.3:n.1242-83T>C
ENST00000344680.8:c.1023-83T>C (RTN2)	ENSP00000345127.3:n.1023-83T>C
ENST00000401705.5:c.-16+90A>G (PPM1N)	ENSP00000384318.1:n.-16+90A>G
ENST00000430715.6:c.222-83T>C (RTN2)	ENSP00000398178.1:n.222-83T>C
ENST00000587597.5:c.1242-83T>C (RTN2)	ENSP00000468144.1:n.1242-83T>C
ENST00000588036.5:n.80-83T>C (RTN2)
ENST00000589628.1:n.209-83T>C (RTN2)
ENST00000590526.5:c.420-83T>C (RTN2)	ENSP00000466619.1:n.420-83T>C
ENST00000590746.5:n.62-2956T>C (RTN2)
ENST00000591286.5:c.*240-83T>C (RTN2)	ENSP00000467863.1:n.*240-83T>C
ENST00000593129.1:n.35T>C (RTN2)