Canonical Allele Identifier: CA2584193018

Gene: CCNE1

Linked Data

• gnomAD v4: 19-29813479-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29813479C>A , CM000681.2:g.29813479C>A	GRCh38
NC_000019.9:g.30304386C>A , CM000681.1:g.30304386C>A	GRCh37
NC_000019.8:g.34996226C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262643.8:c.180+442C>A MANE Select	ENSP00000262643.3:n.180+442C>A
ENST00000262643.7:c.180+442C>A	ENSP00000262643.3:n.180+442C>A
ENST00000357943.9:c.135+442C>A	ENSP00000350625.6:n.135+442C>A
ENST00000444983.6:c.135+442C>A	ENSP00000410179.2:n.135+442C>A
ENST00000575243.5:c.171+442C>A	ENSP00000459024.1:n.171+442C>A
NM_001238.2:c.180+442C>A	NP_001229.1:n.180+442C>A
XM_005259370.2:c.180+442C>A	XP_005259427.1:n.180+442C>A
XM_006723457.2:c.135+442C>A	XP_006723520.1:n.135+442C>A
XM_011527440.1:c.171+442C>A	XP_011525742.1:n.171+442C>A
NM_001238.3:c.180+442C>A	NP_001229.1:n.180+442C>A
NM_001322259.1:c.180+442C>A	NP_001309188.1:n.180+442C>A
NM_001322261.1:c.180+442C>A	NP_001309190.1:n.180+442C>A
NM_001322262.1:c.135+442C>A	NP_001309191.1:n.135+442C>A
XM_011527440.2:c.171+442C>A	XP_011525742.1:n.171+442C>A
NM_001238.4:c.180+442C>A MANE Select	NP_001229.1:n.180+442C>A
NM_001322259.2:c.180+442C>A	NP_001309188.1:n.180+442C>A
NM_001322261.2:c.180+442C>A	NP_001309190.1:n.180+442C>A
NM_001322262.2:c.135+442C>A	NP_001309191.1:n.135+442C>A