Canonical Allele Identifier: CA2584192965
Gene: CCNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29813461_29813468del , CM000681.2:g.29813461_29813468del GRCh38
NC_000019.9:g.30304368_30304375del , CM000681.1:g.30304368_30304375del GRCh37
NC_000019.8:g.34996208_34996215del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262643.8:c.180+424_180+431del MANE Select ENSP00000262643.3:n.180+424_180+431del
ENST00000262643.7:c.180+424_180+431del ENSP00000262643.3:n.180+424_180+431del
ENST00000357943.9:c.135+424_135+431del ENSP00000350625.6:n.135+424_135+431del
ENST00000444983.6:c.135+424_135+431del ENSP00000410179.2:n.135+424_135+431del
ENST00000575243.5:c.171+424_171+431del ENSP00000459024.1:n.171+424_171+431del
NM_001238.2:c.180+424_180+431del NP_001229.1:n.180+424_180+431del
XM_005259370.2:c.180+424_180+431del XP_005259427.1:n.180+424_180+431del
XM_006723457.2:c.135+424_135+431del XP_006723520.1:n.135+424_135+431del
XM_011527440.1:c.171+424_171+431del XP_011525742.1:n.171+424_171+431del
NM_001238.3:c.180+424_180+431del NP_001229.1:n.180+424_180+431del
NM_001322259.1:c.180+424_180+431del NP_001309188.1:n.180+424_180+431del
NM_001322261.1:c.180+424_180+431del NP_001309190.1:n.180+424_180+431del
NM_001322262.1:c.135+424_135+431del NP_001309191.1:n.135+424_135+431del
XM_011527440.2:c.171+424_171+431del XP_011525742.1:n.171+424_171+431del
NM_001238.4:c.180+424_180+431del MANE Select NP_001229.1:n.180+424_180+431del
NM_001322259.2:c.180+424_180+431del NP_001309188.1:n.180+424_180+431del
NM_001322261.2:c.180+424_180+431del NP_001309190.1:n.180+424_180+431del
NM_001322262.2:c.135+424_135+431del NP_001309191.1:n.135+424_135+431del