Canonical Allele Identifier: CA2011604079
Gene: NINJ2 HGNC NCBI
NINJ2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.631795G>C , CM000674.2:g.631795G>C GRCh38
NC_000012.11:g.740961G>C , CM000674.1:g.740961G>C GRCh37
NC_000012.10:g.611222G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305108.10:c.33+31533C>G (NINJ2) MANE Select ENSP00000307552.5:n.33+31533C>G
ENST00000305108.9:c.33+31533C>G (NINJ2) ENSP00000307552.5:n.33+31533C>G
ENST00000662884.1:c.171+31533C>G (NINJ2) ENSP00000499548.1:n.171+31533C>G
ENST00000305108.8:c.171+31533C>G (NINJ2) ENSP00000307552.4:n.171+31533C>G
ENST00000433832.2:c.-76+11716C>G (NINJ2) ENSP00000415158.2:n.-76+11716C>G
ENST00000537416.1:n.175+11716C>G (NINJ2)
ENST00000542920.1:c.-76+11716C>G (NINJ2) ENSP00000438831.1:n.-76+11716C>G
NM_001294346.1:c.-76+11716C>G (NINJ2) NP_001281275.1:n.-76+11716C>G
NM_016533.5:c.171+31533C>G (NINJ2) NP_057617.2:n.171+31533C>G
NR_122124.1:n.96-419G>C (NINJ2-AS1)
NM_001294346.2:c.-76+11716C>G (NINJ2) NP_001281275.1:n.-76+11716C>G
NM_001367996.1:c.-76+9565C>G (NINJ2) NP_001354925.1:n.-76+9565C>G
NM_016533.6:c.33+31533C>G (NINJ2) MANE Select NP_057617.3:n.33+31533C>G
NR_160428.1:n.126+11716C>G (NINJ2)