Canonical Allele Identifier: CA2642019516

Gene: CCBE1

Linked Data

• gnomAD v4: 18-59438286-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59438288del , CM000680.2:g.59438288del	GRCh38
NC_000018.9:g.57105520del , CM000680.1:g.57105520del	GRCh37
NC_000018.8:g.55256500del	NCBI36
NG_016990.1:g.264126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589419.2:n.955-141del
ENST00000650467.2:c.730-141del	ENSP00000496897.2:n.730-141del
ENST00000695903.1:c.1065-141del	ENSP00000512255.1:n.1065-141del
ENST00000695904.1:c.1065-141del	ENSP00000512259.1:n.1065-141del
ENST00000439986.9:c.952-141del MANE Select	ENSP00000404464.2:n.952-141del
ENST00000589116.2:n.660-141del
ENST00000649564.1:c.952-141del	ENSP00000497183.1:n.952-141del
ENST00000650467.1:c.608-141del
ENST00000398179.3:c.742-141del	ENSP00000381241.3:n.742-141del
ENST00000439986.8:c.952-141del	ENSP00000404464.2:n.952-141del
ENST00000589116.1:n.660-141del
NM_133459.3:c.952-141del	NP_597716.1:n.952-141del
XM_005266648.2:c.952-141del	XP_005266705.1:n.952-141del
NM_133459.4:c.952-141del MANE Select	NP_597716.1:n.952-141del
XM_017025556.1:c.1065-141del	XP_016881045.1:n.1065-141del
XM_017025557.1:c.1065-141del	XP_016881046.1:n.1065-141del
XM_017025558.1:c.952-141del	XP_016881047.1:n.952-141del
XM_024451091.1:c.952-141del	XP_024306859.1:n.952-141del
XR_001753142.1:n.1904-141del