Canonical Allele Identifier: CA881269556

Gene: CCNE1

Linked Data

• dbSNP Id: rs1292425835
• MyVariant Identifiers: chr19:g.30304546_30304548del (hg19) ; chr19:g.29813639_29813641del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29813639_29813641del , CM000681.2:g.29813639_29813641del	GRCh38
NC_000019.9:g.30304546_30304548del , CM000681.1:g.30304546_30304548del	GRCh37
NC_000019.8:g.34996386_34996388del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262643.8:c.180+602_180+604del MANE Select	ENSP00000262643.3:n.180+602_180+604del
ENST00000262643.7:c.180+602_180+604del	ENSP00000262643.3:n.180+602_180+604del
ENST00000357943.9:c.135+602_135+604del	ENSP00000350625.6:n.135+602_135+604del
ENST00000444983.6:c.135+602_135+604del	ENSP00000410179.2:n.135+602_135+604del
ENST00000575243.5:c.171+602_171+604del	ENSP00000459024.1:n.171+602_171+604del
NM_001238.2:c.180+602_180+604del	NP_001229.1:n.180+602_180+604del
XM_005259370.2:c.180+602_180+604del	XP_005259427.1:n.180+602_180+604del
XM_006723457.2:c.135+602_135+604del	XP_006723520.1:n.135+602_135+604del
XM_011527440.1:c.171+602_171+604del	XP_011525742.1:n.171+602_171+604del
NM_001238.3:c.180+602_180+604del	NP_001229.1:n.180+602_180+604del
NM_001322259.1:c.180+602_180+604del	NP_001309188.1:n.180+602_180+604del
NM_001322261.1:c.180+602_180+604del	NP_001309190.1:n.180+602_180+604del
NM_001322262.1:c.135+602_135+604del	NP_001309191.1:n.135+602_135+604del
XM_011527440.2:c.171+602_171+604del	XP_011525742.1:n.171+602_171+604del
NM_001238.4:c.180+602_180+604del MANE Select	NP_001229.1:n.180+602_180+604del
NM_001322259.2:c.180+602_180+604del	NP_001309188.1:n.180+602_180+604del
NM_001322261.2:c.180+602_180+604del	NP_001309190.1:n.180+602_180+604del
NM_001322262.2:c.135+602_135+604del	NP_001309191.1:n.135+602_135+604del