Canonical Allele Identifier: CA2306909798

Gene: CCBE1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59438172_59438173delinsCT , CM000680.2:g.59438172_59438173delinsCT	GRCh38
NC_000018.9:g.57105404_57105405delinsCT , CM000680.1:g.57105404_57105405delinsCT	GRCh37
NC_000018.8:g.55256384_55256385delinsCT	NCBI36
NG_016990.1:g.264240_264241delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000589419.2:n.955-27_955-26delinsAG
ENST00000650467.2:c.730-27_730-26delinsAG	ENSP00000496897.2:n.730-27_730-26delinsAG
ENST00000695903.1:c.1065-27_1065-26delinsAG	ENSP00000512255.1:n.1065-27_1065-26delinsAG
ENST00000695904.1:c.1065-27_1065-26delinsAG	ENSP00000512259.1:n.1065-27_1065-26delinsAG
ENST00000439986.9:c.952-27_952-26delinsAG MANE Select	ENSP00000404464.2:n.952-27_952-26delinsAG
ENST00000589116.2:n.660-27_660-26delinsAG
ENST00000649564.1:c.952-27_952-26delinsAG	ENSP00000497183.1:n.952-27_952-26delinsAG
ENST00000650467.1:c.608-27_608-26delinsAG
ENST00000398179.3:c.742-27_742-26delinsAG	ENSP00000381241.3:n.742-27_742-26delinsAG
ENST00000439986.8:c.952-27_952-26delinsAG	ENSP00000404464.2:n.952-27_952-26delinsAG
ENST00000589116.1:n.660-27_660-26delinsAG
NM_133459.3:c.952-27_952-26delinsAG	NP_597716.1:n.952-27_952-26delinsAG
XM_005266648.2:c.952-27_952-26delinsAG	XP_005266705.1:n.952-27_952-26delinsAG
NM_133459.4:c.952-27_952-26delinsAG MANE Select	NP_597716.1:n.952-27_952-26delinsAG
XM_017025556.1:c.1065-27_1065-26delinsAG	XP_016881045.1:n.1065-27_1065-26delinsAG
XM_017025557.1:c.1065-27_1065-26delinsAG	XP_016881046.1:n.1065-27_1065-26delinsAG
XM_017025558.1:c.952-27_952-26delinsAG	XP_016881047.1:n.952-27_952-26delinsAG
XM_024451091.1:c.952-27_952-26delinsAG	XP_024306859.1:n.952-27_952-26delinsAG
XR_001753142.1:n.1904-27_1904-26delinsAG