Canonical Allele Identifier: CA406356557

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992701G>C (hg19) ; chr19:g.45489443G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489443G>C , CM000681.2:g.45489443G>C	GRCh38
NC_000019.9:g.45992701G>C , CM000681.1:g.45992701G>C	GRCh37
NC_000019.8:g.50684541G>C	NCBI36
NG_032157.1:g.12611C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245923.9:c.1144C>G (RTN2) MANE Select	ENSP00000245923.3:p.His382Asp
ENST00000245923.8:c.1144C>G (RTN2)	ENSP00000245923.3:p.His382Asp
ENST00000344680.8:c.925C>G (RTN2)	ENSP00000345127.3:p.His309Asp
ENST00000401705.5:c.-16+464G>C (PPM1N)	ENSP00000384318.1:n.-16+464G>C
ENST00000430715.6:c.124C>G (RTN2)	ENSP00000398178.1:p.His42Asp
ENST00000587597.5:c.1144C>G (RTN2)	ENSP00000468144.1:p.His382Asp
ENST00000588036.5:n.80-457C>G (RTN2)
ENST00000589628.1:n.111C>G (RTN2)
ENST00000590526.5:c.322C>G (RTN2)	ENSP00000466619.1:p.His108Asp
ENST00000590746.5:n.62-3330C>G (RTN2)
ENST00000591286.5:c.*142C>G (RTN2)	ENSP00000467863.1:n.*142C>G
NM_005619.4:c.1144C>G (RTN2)	NP_005610.1:p.His382Asp
NM_206900.2:c.925C>G (RTN2)	NP_996783.1:p.His309Asp
NM_206901.2:c.124C>G (RTN2)	NP_996784.1:p.His42Asp
NM_005619.5:c.1144C>G (RTN2) MANE Select	NP_005610.1:p.His382Asp
NM_206900.3:c.925C>G (RTN2)	NP_996783.1:p.His309Asp
NM_206901.3:c.124C>G (RTN2)	NP_996784.1:p.His42Asp