Canonical Allele Identifier: CA2079393954

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882875T= , CM000675.2:g.24882875T= GRCh38
NC_000013.10:g.25457013T= , CM000675.1:g.25457013T= GRCh37
NC_000013.9:g.24355013T= NCBI36
NG_009165.2:g.45073A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*302A= (CENPJ) MANE Select ENSP00000371308.4:n.*302A=
ENST00000616936.4:c.*973A= (CENPJ) ENSP00000477511.1:n.*973A=
NM_018451.4:c.*302A= (CENPJ) NP_060921.3:n.*302A=
NR_047594.1:n.4631A= (CENPJ)
NR_047595.1:n.4429A= (CENPJ)
XM_011535156.1:c.*10+3580T= (RNF17) XP_011533458.1:n.*10+3580T=
XM_011535156.2:c.*10+3580T= (RNF17) XP_011533458.1:n.*10+3580T=
NM_018451.5:c.*302A= (CENPJ) MANE Select NP_060921.3:n.*302A=
NR_047594.2:n.4603A= (CENPJ)
NR_047595.2:n.4401A= (CENPJ)