Canonical Allele Identifier: CA504064707

Gene: CCBE1

Linked Data

• COSMIC: COSM3937770
• MyVariant Identifiers: chr18:g.57136709A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59469477A>G , CM000680.2:g.59469477A>G	GRCh38
NC_000018.9:g.57136709A>G , CM000680.1:g.57136709A>G	GRCh37
NC_000018.8:g.55287689A>G	NCBI36
NG_016990.1:g.232936T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000589419.2:n.399T>C
ENST00000650467.2:c.396T>C	ENSP00000496897.2:p.Cys132=
ENST00000695903.1:c.396T>C	ENSP00000512255.1:p.Cys132=
ENST00000695904.1:c.396T>C	ENSP00000512259.1:p.Cys132=
ENST00000439986.9:c.396T>C MANE Select	ENSP00000404464.2:p.Cys132=
ENST00000649564.1:c.396T>C	ENSP00000497183.1:p.Cys132=
ENST00000650467.1:c.274T>C
ENST00000398179.3:c.186T>C	ENSP00000381241.3:p.Cys62=
ENST00000439986.8:c.396T>C	ENSP00000404464.2:p.Cys132=
ENST00000589419.1:c.-178T>C	ENSP00000467710.1:n.-178T>C
NM_133459.3:c.396T>C	NP_597716.1:p.Cys132=
XM_005266648.2:c.396T>C	XP_005266705.1:p.Cys132=
NM_133459.4:c.396T>C MANE Select	NP_597716.1:p.Cys132=
XM_017025556.1:c.396T>C	XP_016881045.1:p.Cys132=
XM_017025557.1:c.396T>C	XP_016881046.1:p.Cys132=
XM_017025558.1:c.396T>C	XP_016881047.1:p.Cys132=
XM_024451091.1:c.396T>C	XP_024306859.1:p.Cys132=
XR_001753142.1:n.1235T>C