Canonical Allele Identifier: CA2079394014

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882980A= , CM000675.2:g.24882980A= GRCh38
NC_000013.10:g.25457118A= , CM000675.1:g.25457118A= GRCh37
NC_000013.9:g.24355118A= NCBI36
NG_009165.2:g.44968T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*197T= (CENPJ) MANE Select ENSP00000371308.4:n.*197T=
ENST00000616936.4:c.*868T= (CENPJ) ENSP00000477511.1:n.*868T=
NM_018451.4:c.*197T= (CENPJ) NP_060921.3:n.*197T=
NR_047594.1:n.4526T= (CENPJ)
NR_047595.1:n.4324T= (CENPJ)
XM_011535156.1:c.*10+3685A= (RNF17) XP_011533458.1:n.*10+3685A=
XM_011535156.2:c.*10+3685A= (RNF17) XP_011533458.1:n.*10+3685A=
NM_018451.5:c.*197T= (CENPJ) MANE Select NP_060921.3:n.*197T=
NR_047594.2:n.4498T= (CENPJ)
NR_047595.2:n.4296T= (CENPJ)