Canonical Allele Identifier: CA2585808912

Gene: RTN2 PPM1N

Linked Data

• gnomAD v4: 19-45489397-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45489400del , CM000681.2:g.45489400del	GRCh38
NC_000019.9:g.45992658del , CM000681.1:g.45992658del	GRCh37
NC_000019.8:g.50684498del	NCBI36
NG_032157.1:g.12656del

Transcript Alleles

HGVS	Amino-acid change
ENST00000245923.9:c.1189del (RTN2) MANE Select	ENSP00000245923.3:p.Tyr397ThrfsTer27
ENST00000245923.8:c.1189del (RTN2)	ENSP00000245923.3:p.Tyr397ThrfsTer27
ENST00000344680.8:c.970del (RTN2)	ENSP00000345127.3:p.Tyr324ThrfsTer27
ENST00000401705.5:c.-16+421del (PPM1N)	ENSP00000384318.1:n.-16+421del
ENST00000430715.6:c.169del (RTN2)	ENSP00000398178.1:p.Tyr57ThrfsTer27
ENST00000587597.5:c.1189del (RTN2)	ENSP00000468144.1:p.Tyr397ThrfsTer27
ENST00000588036.5:n.80-412del (RTN2)
ENST00000589628.1:n.156del (RTN2)
ENST00000590526.5:c.367del (RTN2)	ENSP00000466619.1:p.Tyr123ThrfsTer27
ENST00000590746.5:n.62-3285del (RTN2)
ENST00000591286.5:c.*187del (RTN2)	ENSP00000467863.1:n.*187del
NM_005619.4:c.1189del (RTN2)	NP_005610.1:p.Tyr397ThrfsTer27
NM_206900.2:c.970del (RTN2)	NP_996783.1:p.Tyr324ThrfsTer27
NM_206901.2:c.169del (RTN2)	NP_996784.1:p.Tyr57ThrfsTer27
NM_005619.5:c.1189del (RTN2) MANE Select	NP_005610.1:p.Tyr397ThrfsTer27
NM_206900.3:c.970del (RTN2)	NP_996783.1:p.Tyr324ThrfsTer27
NM_206901.3:c.169del (RTN2)	NP_996784.1:p.Tyr57ThrfsTer27