Canonical Allele Identifier: CA507818707

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992771T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489513T>G , CM000681.2:g.45489513T>G	GRCh38
NC_000019.9:g.45992771T>G , CM000681.1:g.45992771T>G	GRCh37
NC_000019.8:g.50684611T>G	NCBI36
NG_032157.1:g.12541A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.1074A>C (RTN2) MANE Select	ENSP00000245923.3:p.Gly358=
ENST00000245923.8:c.1074A>C (RTN2)	ENSP00000245923.3:p.Gly358=
ENST00000344680.8:c.855A>C (RTN2)	ENSP00000345127.3:p.Gly285=
ENST00000401705.5:c.-16+534T>G (PPM1N)	ENSP00000384318.1:n.-16+534T>G
ENST00000430715.6:c.54A>C (RTN2)	ENSP00000398178.1:p.Gly18=
ENST00000587597.5:c.1074A>C (RTN2)	ENSP00000468144.1:p.Gly358=
ENST00000588036.5:n.80-527A>C (RTN2)
ENST00000589628.1:n.41A>C (RTN2)
ENST00000590526.5:c.252A>C (RTN2)	ENSP00000466619.1:p.Gly84=
ENST00000590746.5:n.62-3400A>C (RTN2)
ENST00000591286.5:c.*72A>C (RTN2)	ENSP00000467863.1:n.*72A>C
NM_005619.4:c.1074A>C (RTN2)	NP_005610.1:p.Gly358=
NM_206900.2:c.855A>C (RTN2)	NP_996783.1:p.Gly285=
NM_206901.2:c.54A>C (RTN2)	NP_996784.1:p.Gly18=
NM_005619.5:c.1074A>C (RTN2) MANE Select	NP_005610.1:p.Gly358=
NM_206900.3:c.855A>C (RTN2)	NP_996783.1:p.Gly285=
NM_206901.3:c.54A>C (RTN2)	NP_996784.1:p.Gly18=