Canonical Allele Identifier: CA2622386432

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882853_24882858del , CM000675.2:g.24882853_24882858del GRCh38
NC_000013.10:g.25456991_25456996del , CM000675.1:g.25456991_25456996del GRCh37
NC_000013.9:g.24354991_24354996del NCBI36
NG_009165.2:g.45090_45095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*319_*324del (CENPJ) MANE Select ENSP00000371308.4:n.*319_*324del
ENST00000616936.4:c.*990_*995del (CENPJ) ENSP00000477511.1:n.*990_*995del
NM_018451.4:c.*319_*324del (CENPJ) NP_060921.3:n.*319_*324del
NR_047594.1:n.4648_4653del (CENPJ)
NR_047595.1:n.4446_4451del (CENPJ)
XM_011535156.1:c.*10+3558_*10+3563del (RNF17) XP_011533458.1:n.*10+3558_*10+3563del
XM_011535156.2:c.*10+3558_*10+3563del (RNF17) XP_011533458.1:n.*10+3558_*10+3563del
NM_018451.5:c.*319_*324del (CENPJ) MANE Select NP_060921.3:n.*319_*324del
NR_047594.2:n.4620_4625del (CENPJ)
NR_047595.2:n.4418_4423del (CENPJ)