Canonical Allele Identifier: CA2306925608

Gene: CCBE1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59469483T= , CM000680.2:g.59469483T=	GRCh38
NC_000018.9:g.57136715T= , CM000680.1:g.57136715T=	GRCh37
NC_000018.8:g.55287695T=	NCBI36
NG_016990.1:g.232930A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000589419.2:n.393A=
ENST00000650467.2:c.390A=	ENSP00000496897.2:p.Pro130=
ENST00000695903.1:c.390A=	ENSP00000512255.1:p.Pro130=
ENST00000695904.1:c.390A=	ENSP00000512259.1:p.Pro130=
ENST00000439986.9:c.390A= MANE Select	ENSP00000404464.2:p.Pro130=
ENST00000649564.1:c.390A=	ENSP00000497183.1:p.Pro130=
ENST00000650467.1:c.268A=
ENST00000398179.3:c.180A=	ENSP00000381241.3:p.Pro60=
ENST00000439986.8:c.390A=	ENSP00000404464.2:p.Pro130=
ENST00000589419.1:c.-184A=	ENSP00000467710.1:n.-184A=
NM_133459.3:c.390A=	NP_597716.1:p.Pro130=
XM_005266648.2:c.390A=	XP_005266705.1:p.Pro130=
NM_133459.4:c.390A= MANE Select	NP_597716.1:p.Pro130=
XM_017025556.1:c.390A=	XP_016881045.1:p.Pro130=
XM_017025557.1:c.390A=	XP_016881046.1:p.Pro130=
XM_017025558.1:c.390A=	XP_016881047.1:p.Pro130=
XM_024451091.1:c.390A=	XP_024306859.1:p.Pro130=
XR_001753142.1:n.1229A=