Canonical Allele Identifier: CA507818493

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992657A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489399A>G , CM000681.2:g.45489399A>G	GRCh38
NC_000019.9:g.45992657A>G , CM000681.1:g.45992657A>G	GRCh37
NC_000019.8:g.50684497A>G	NCBI36
NG_032157.1:g.12655T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1188T>C (RTN2) MANE Select	ENSP00000245923.3:p.Val396=
ENST00000245923.8:c.1188T>C (RTN2)	ENSP00000245923.3:p.Val396=
ENST00000344680.8:c.969T>C (RTN2)	ENSP00000345127.3:p.Val323=
ENST00000401705.5:c.-16+420A>G (PPM1N)	ENSP00000384318.1:n.-16+420A>G
ENST00000430715.6:c.168T>C (RTN2)	ENSP00000398178.1:p.Val56=
ENST00000587597.5:c.1188T>C (RTN2)	ENSP00000468144.1:p.Val396=
ENST00000588036.5:n.80-413T>C (RTN2)
ENST00000589628.1:n.155T>C (RTN2)
ENST00000590526.5:c.366T>C (RTN2)	ENSP00000466619.1:p.Val122=
ENST00000590746.5:n.62-3286T>C (RTN2)
ENST00000591286.5:c.*186T>C (RTN2)	ENSP00000467863.1:n.*186T>C
NM_005619.4:c.1188T>C (RTN2)	NP_005610.1:p.Val396=
NM_206900.2:c.969T>C (RTN2)	NP_996783.1:p.Val323=
NM_206901.2:c.168T>C (RTN2)	NP_996784.1:p.Val56=
NM_005619.5:c.1188T>C (RTN2) MANE Select	NP_005610.1:p.Val396=
NM_206900.3:c.969T>C (RTN2)	NP_996783.1:p.Val323=
NM_206901.3:c.168T>C (RTN2)	NP_996784.1:p.Val56=