Canonical Allele Identifier: CA406362609

Gene: RTN2 PPM1N

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45494887G>T , CM000681.2:g.45494887G>T	GRCh38
NC_000019.9:g.45998145G>T , CM000681.1:g.45998145G>T	GRCh37
NC_000019.8:g.50689985G>T	NCBI36
NG_032157.1:g.7167C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005619.5:c.198C>A (RTN2) MANE Select	NP_005610.1:p.Tyr66Ter
ENST00000245923.9:c.198C>A (RTN2) MANE Select	ENSP00000245923.3:p.Tyr66Ter
NM_005619.4:c.198C>A (RTN2)	NP_005610.1:p.Tyr66Ter
NM_206900.2:c.198C>A (RTN2)	NP_996783.1:p.Tyr66Ter
NM_206900.3:c.198C>A (RTN2)	NP_996783.1:p.Tyr66Ter
ENST00000245923.8:c.198C>A (RTN2)	ENSP00000245923.3:p.Tyr66Ter
ENST00000344680.8:c.198C>A (RTN2)	ENSP00000345127.3:p.Tyr66Ter
ENST00000401705.5:c.-15-5062G>T (PPM1N)	ENSP00000384318.1:n.-15-5062G>T
ENST00000587597.5:c.198C>A (RTN2)	ENSP00000468144.1:p.Tyr66Ter
ENST00000589384.1:n.257C>A (RTN2)
ENST00000590526.5:c.-625C>A (RTN2)	ENSP00000466619.1:n.-625C>A
ENST00000591286.5:c.198C>A (RTN2)	ENSP00000467863.1:p.Tyr66Ter
ENST00000592064.1:n.19C>A (RTN2)