Canonical Allele Identifier: CA406357017

Gene: RTN2 PPM1N

Linked Data

• MyVariant Identifiers: chr19:g.45992750C>G (hg19) ; chr19:g.45489492C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489492C>G , CM000681.2:g.45489492C>G	GRCh38
NC_000019.9:g.45992750C>G , CM000681.1:g.45992750C>G	GRCh37
NC_000019.8:g.50684590C>G	NCBI36
NG_032157.1:g.12562G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1095G>C (RTN2) MANE Select	ENSP00000245923.3:p.Met365Ile
ENST00000245923.8:c.1095G>C (RTN2)	ENSP00000245923.3:p.Met365Ile
ENST00000344680.8:c.876G>C (RTN2)	ENSP00000345127.3:p.Met292Ile
ENST00000401705.5:c.-16+513C>G (PPM1N)	ENSP00000384318.1:n.-16+513C>G
ENST00000430715.6:c.75G>C (RTN2)	ENSP00000398178.1:p.Met25Ile
ENST00000587597.5:c.1095G>C (RTN2)	ENSP00000468144.1:p.Met365Ile
ENST00000588036.5:n.80-506G>C (RTN2)
ENST00000589628.1:n.62G>C (RTN2)
ENST00000590526.5:c.273G>C (RTN2)	ENSP00000466619.1:p.Met91Ile
ENST00000590746.5:n.62-3379G>C (RTN2)
ENST00000591286.5:c.*93G>C (RTN2)	ENSP00000467863.1:n.*93G>C
NM_005619.4:c.1095G>C (RTN2)	NP_005610.1:p.Met365Ile
NM_206900.2:c.876G>C (RTN2)	NP_996783.1:p.Met292Ile
NM_206901.2:c.75G>C (RTN2)	NP_996784.1:p.Met25Ile
NM_005619.5:c.1095G>C (RTN2) MANE Select	NP_005610.1:p.Met365Ile
NM_206900.3:c.876G>C (RTN2)	NP_996783.1:p.Met292Ile
NM_206901.3:c.75G>C (RTN2)	NP_996784.1:p.Met25Ile