Canonical Allele Identifier: CA402592415
Gene: CCBE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59469481T>A , CM000680.2:g.59469481T>A GRCh38
NC_000018.9:g.57136713T>A , CM000680.1:g.57136713T>A GRCh37
NC_000018.8:g.55287693T>A NCBI36
NG_016990.1:g.232932A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000589419.2:n.395A>T
ENST00000650467.2:c.392A>T ENSP00000496897.2:p.Tyr131Phe
ENST00000695903.1:c.392A>T ENSP00000512255.1:p.Tyr131Phe
ENST00000695904.1:c.392A>T ENSP00000512259.1:p.Tyr131Phe
ENST00000439986.9:c.392A>T MANE Select ENSP00000404464.2:p.Tyr131Phe
ENST00000649564.1:c.392A>T ENSP00000497183.1:p.Tyr131Phe
ENST00000650467.1:c.270A>T
ENST00000398179.3:c.182A>T ENSP00000381241.3:p.Tyr61Phe
ENST00000439986.8:c.392A>T ENSP00000404464.2:p.Tyr131Phe
ENST00000589419.1:c.-182A>T ENSP00000467710.1:n.-182A>T
NM_133459.3:c.392A>T NP_597716.1:p.Tyr131Phe
XM_005266648.2:c.392A>T XP_005266705.1:p.Tyr131Phe
NM_133459.4:c.392A>T MANE Select NP_597716.1:p.Tyr131Phe
XM_017025556.1:c.392A>T XP_016881045.1:p.Tyr131Phe
XM_017025557.1:c.392A>T XP_016881046.1:p.Tyr131Phe
XM_017025558.1:c.392A>T XP_016881047.1:p.Tyr131Phe
XM_024451091.1:c.392A>T XP_024306859.1:p.Tyr131Phe
XR_001753142.1:n.1231A>T