Canonical Allele Identifier: CA14674032
Gene: CCNE1 HGNC NCBI

Linked Data

dbSNP Id: rs997669

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29813576T>C , CM000681.2:g.29813576T>C GRCh38
NC_000019.9:g.30304483T>C , CM000681.1:g.30304483T>C GRCh37
NC_000019.8:g.34996323T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262643.8:c.180+539T>C MANE Select ENSP00000262643.3:p.=
ENST00000262643.7:c.180+539T>C ENSP00000262643.3:p.=
ENST00000357943.9:c.135+539T>C ENSP00000350625.6:p.=
ENST00000444983.6:c.135+539T>C ENSP00000410179.2:p.=
ENST00000575243.5:c.171+539T>C ENSP00000459024.1:p.=
NM_001238.2:c.180+539T>C NP_001229.1:p.=
XM_005259370.2:c.180+539T>C XP_005259427.1:p.=
XM_006723457.2:c.135+539T>C XP_006723520.1:p.=
XM_011527440.1:c.171+539T>C XP_011525742.1:p.=
NM_001238.3:c.180+539T>C NP_001229.1:p.=
NM_001322259.1:c.180+539T>C NP_001309188.1:p.=
NM_001322261.1:c.180+539T>C NP_001309190.1:p.=
NM_001322262.1:c.135+539T>C NP_001309191.1:p.=
XM_011527440.2:c.171+539T>C XP_011525742.1:p.=
NM_001238.4:c.180+539T>C MANE Select NP_001229.1:p.=
NM_001322259.2:c.180+539T>C NP_001309188.1:p.=
NM_001322261.2:c.180+539T>C NP_001309190.1:p.=
NM_001322262.2:c.135+539T>C NP_001309191.1:p.=