Canonical Allele Identifier: CA402592405

Gene: CCBE1

Linked Data

• gnomAD v4: 18-59469478-C-A
• MyVariant Identifiers: chr18:g.57136710C>A (hg19) ; chr18:g.59469478C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59469478C>A , CM000680.2:g.59469478C>A	GRCh38
NC_000018.9:g.57136710C>A , CM000680.1:g.57136710C>A	GRCh37
NC_000018.8:g.55287690C>A	NCBI36
NG_016990.1:g.232935G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000589419.2:n.398G>T
ENST00000650467.2:c.395G>T	ENSP00000496897.2:p.Cys132Phe
ENST00000695903.1:c.395G>T	ENSP00000512255.1:p.Cys132Phe
ENST00000695904.1:c.395G>T	ENSP00000512259.1:p.Cys132Phe
ENST00000439986.9:c.395G>T MANE Select	ENSP00000404464.2:p.Cys132Phe
ENST00000649564.1:c.395G>T	ENSP00000497183.1:p.Cys132Phe
ENST00000650467.1:c.273G>T
ENST00000398179.3:c.185G>T	ENSP00000381241.3:p.Cys62Phe
ENST00000439986.8:c.395G>T	ENSP00000404464.2:p.Cys132Phe
ENST00000589419.1:c.-179G>T	ENSP00000467710.1:n.-179G>T
NM_133459.3:c.395G>T	NP_597716.1:p.Cys132Phe
XM_005266648.2:c.395G>T	XP_005266705.1:p.Cys132Phe
NM_133459.4:c.395G>T MANE Select	NP_597716.1:p.Cys132Phe
XM_017025556.1:c.395G>T	XP_016881045.1:p.Cys132Phe
XM_017025557.1:c.395G>T	XP_016881046.1:p.Cys132Phe
XM_017025558.1:c.395G>T	XP_016881047.1:p.Cys132Phe
XM_024451091.1:c.395G>T	XP_024306859.1:p.Cys132Phe
XR_001753142.1:n.1234G>T