Canonical Allele Identifier: CA2306909751

Gene: CCBE1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59438085G= , CM000680.2:g.59438085G=	GRCh38
NC_000018.9:g.57105317G= , CM000680.1:g.57105317G=	GRCh37
NC_000018.8:g.55256297G=	NCBI36
NG_016990.1:g.264328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589419.2:n.990+26C=
ENST00000650467.2:c.765+26C=	ENSP00000496897.2:n.765+26C=
ENST00000695903.1:c.*22C=	ENSP00000512255.1:n.*22C=
ENST00000695904.1:c.1100+26C=	ENSP00000512259.1:n.1100+26C=
ENST00000439986.9:c.987+26C= MANE Select	ENSP00000404464.2:n.987+26C=
ENST00000589116.2:n.695+26C=
ENST00000649564.1:c.987+26C=	ENSP00000497183.1:n.987+26C=
ENST00000650467.1:c.643+26C=
ENST00000398179.3:c.777+26C=	ENSP00000381241.3:n.777+26C=
ENST00000439986.8:c.987+26C=	ENSP00000404464.2:n.987+26C=
ENST00000589116.1:n.695+26C=
NM_133459.3:c.987+26C=	NP_597716.1:n.987+26C=
XM_005266648.2:c.987+26C=	XP_005266705.1:n.987+26C=
NM_133459.4:c.987+26C= MANE Select	NP_597716.1:n.987+26C=
XM_017025556.1:c.1100+26C=	XP_016881045.1:n.1100+26C=
XM_017025557.1:c.1100+26C=	XP_016881046.1:n.1100+26C=
XM_017025558.1:c.1013C=	XP_016881047.1:p.Ser338=
XM_024451091.1:c.987+26C=	XP_024306859.1:n.987+26C=
XR_001753142.1:n.1965C=