Canonical Allele Identifier: CA2642019377

Gene: CCBE1

Linked Data

• gnomAD v4: 18-59437981-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59437983del , CM000680.2:g.59437983del	GRCh38
NC_000018.9:g.57105215del , CM000680.1:g.57105215del	GRCh37
NC_000018.8:g.55256195del	NCBI36
NG_016990.1:g.264431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589419.2:n.990+129del
ENST00000650467.2:c.765+129del	ENSP00000496897.2:n.765+129del
ENST00000695903.1:c.*66+59del	ENSP00000512255.1:n.*66+59del
ENST00000695904.1:c.1100+129del	ENSP00000512259.1:n.1100+129del
ENST00000439986.9:c.987+129del MANE Select	ENSP00000404464.2:n.987+129del
ENST00000589116.2:n.695+129del
ENST00000649564.1:c.987+129del	ENSP00000497183.1:n.987+129del
ENST00000650467.1:c.643+129del
ENST00000398179.3:c.777+129del	ENSP00000381241.3:n.777+129del
ENST00000439986.8:c.987+129del	ENSP00000404464.2:n.987+129del
ENST00000589116.1:n.695+129del
NM_133459.3:c.987+129del	NP_597716.1:n.987+129del
XM_005266648.2:c.987+129del	XP_005266705.1:n.987+129del
NM_133459.4:c.987+129del MANE Select	NP_597716.1:n.987+129del
XM_017025556.1:c.1100+129del	XP_016881045.1:n.1100+129del
XM_017025557.1:c.1100+129del	XP_016881046.1:n.1100+129del
XM_017025558.1:c.1057+59del	XP_016881047.1:n.1057+59del
XM_024451091.1:c.987+129del	XP_024306859.1:n.987+129del
XR_001753142.1:n.2009+59del