Canonical Allele Identifier: CA2330967673

Gene: CCNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29813488T= , CM000681.2:g.29813488T=	GRCh38
NC_000019.9:g.30304395T= , CM000681.1:g.30304395T=	GRCh37
NC_000019.8:g.34996235T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262643.8:c.180+451T= MANE Select	ENSP00000262643.3:n.180+451T=
ENST00000262643.7:c.180+451T=	ENSP00000262643.3:n.180+451T=
ENST00000357943.9:c.135+451T=	ENSP00000350625.6:n.135+451T=
ENST00000444983.6:c.135+451T=	ENSP00000410179.2:n.135+451T=
ENST00000575243.5:c.171+451T=	ENSP00000459024.1:n.171+451T=
NM_001238.2:c.180+451T=	NP_001229.1:n.180+451T=
XM_005259370.2:c.180+451T=	XP_005259427.1:n.180+451T=
XM_006723457.2:c.135+451T=	XP_006723520.1:n.135+451T=
XM_011527440.1:c.171+451T=	XP_011525742.1:n.171+451T=
NM_001238.3:c.180+451T=	NP_001229.1:n.180+451T=
NM_001322259.1:c.180+451T=	NP_001309188.1:n.180+451T=
NM_001322261.1:c.180+451T=	NP_001309190.1:n.180+451T=
NM_001322262.1:c.135+451T=	NP_001309191.1:n.135+451T=
XM_011527440.2:c.171+451T=	XP_011525742.1:n.171+451T=
NM_001238.4:c.180+451T= MANE Select	NP_001229.1:n.180+451T=
NM_001322259.2:c.180+451T=	NP_001309188.1:n.180+451T=
NM_001322261.2:c.180+451T=	NP_001309190.1:n.180+451T=
NM_001322262.2:c.135+451T=	NP_001309191.1:n.135+451T=