Canonical Allele Identifier: CA402591617

Gene: CCBE1

Linked Data

• MyVariant Identifiers: chr18:g.57134015T>A (hg19) ; chr18:g.59466783T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59466783T>A , CM000680.2:g.59466783T>A	GRCh38
NC_000018.9:g.57134015T>A , CM000680.1:g.57134015T>A	GRCh37
NC_000018.8:g.55284995T>A	NCBI36
NG_016990.1:g.235630A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000589419.2:n.512A>T
ENST00000650467.2:c.509A>T	ENSP00000496897.2:p.Asp170Val
ENST00000695903.1:c.509A>T	ENSP00000512255.1:p.Asp170Val
ENST00000695904.1:c.509A>T	ENSP00000512259.1:p.Asp170Val
ENST00000439986.9:c.509A>T MANE Select	ENSP00000404464.2:p.Asp170Val
ENST00000649564.1:c.509A>T	ENSP00000497183.1:p.Asp170Val
ENST00000650467.1:c.387A>T
ENST00000398179.3:c.299A>T	ENSP00000381241.3:p.Asp100Val
ENST00000439986.8:c.509A>T	ENSP00000404464.2:p.Asp170Val
ENST00000589419.1:c.-65A>T	ENSP00000467710.1:n.-65A>T
NM_133459.3:c.509A>T	NP_597716.1:p.Asp170Val
XM_005266648.2:c.509A>T	XP_005266705.1:p.Asp170Val
NM_133459.4:c.509A>T MANE Select	NP_597716.1:p.Asp170Val
XM_017025556.1:c.509A>T	XP_016881045.1:p.Asp170Val
XM_017025557.1:c.509A>T	XP_016881046.1:p.Asp170Val
XM_017025558.1:c.509A>T	XP_016881047.1:p.Asp170Val
XM_024451091.1:c.509A>T	XP_024306859.1:p.Asp170Val
XR_001753142.1:n.1348A>T