Canonical Allele Identifier: CA2798539595

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882981G>A , CM000675.2:g.24882981G>A GRCh38
NC_000013.10:g.25457119G>A , CM000675.1:g.25457119G>A GRCh37
NC_000013.9:g.24355119G>A NCBI36
NG_009165.2:g.44967C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*196C>T (CENPJ) MANE Select ENSP00000371308.4:n.*196C>T
ENST00000616936.4:c.*867C>T (CENPJ) ENSP00000477511.1:n.*867C>T
NM_018451.4:c.*196C>T (CENPJ) NP_060921.3:n.*196C>T
NR_047594.1:n.4525C>T (CENPJ)
NR_047595.1:n.4323C>T (CENPJ)
XM_011535156.1:c.*10+3686G>A (RNF17) XP_011533458.1:n.*10+3686G>A
XM_011535156.2:c.*10+3686G>A (RNF17) XP_011533458.1:n.*10+3686G>A
NM_018451.5:c.*196C>T (CENPJ) MANE Select NP_060921.3:n.*196C>T
NR_047594.2:n.4497C>T (CENPJ)
NR_047595.2:n.4295C>T (CENPJ)