Canonical Allele Identifier: CA2579807929

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43068508_43068509delinsAC , CM000683.2:g.43068508_43068509delinsAC	GRCh38
NG_008938.1:g.12422_12423delinsGT , LRG_777:g.12422_12423delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.316_316+1delinsGT
ENST00000352178.9:c.316_316+1delinsGT
ENST00000359624.7:c.316_316+1delinsGT
ENST00000398158.5:c.316_316+1delinsGT
ENST00000398165.7:c.316_316+1delinsGT
ENST00000441030.5:c.316_316+1delinsGT
ENST00000465732.5:n.495_496delinsGT
ENST00000470912.5:n.576_576+1delinsGT
ENST00000488526.1:n.567_568delinsGT
NM_000071.2:c.316_316+1delinsGT , LRG_777t1:c.316_316+1delinsGT
NM_001178008.1:c.316_316+1delinsGT
NM_001178009.1:c.316_316+1delinsGT
XM_011529777.1:c.316_316+1delinsGT
XM_011529778.1:c.316_316+1delinsGT
XM_011529779.1:c.316_316+1delinsGT
XM_011529781.1:c.316_316+1delinsGT
XM_011529782.1:c.316_316+1delinsGT
NM_001178008.2:c.316_316+1delinsGT
NM_001178009.2:c.316_316+1delinsGT
NM_001320298.1:c.316_316+1delinsGT
XM_011529777.2:c.316_316+1delinsGT
XM_017028491.2:c.316_316+1delinsGT
XM_024452136.1:c.-453_-452delinsGT	XP_024307904.1:n.-453_-452delinsGT
XM_024452137.1:c.-453_-452delinsGT	XP_024307905.1:n.-453_-452delinsGT
XM_024452138.1:c.-731_-730delinsGT	XP_024307906.1:n.-731_-730delinsGT
XM_024452139.1:c.-731_-730delinsGT	XP_024307907.1:n.-731_-730delinsGT
XM_024452140.1:c.-731_-730delinsGT	XP_024307908.1:n.-731_-730delinsGT
XR_001754916.2:n.466_466+1delinsGT
XR_001754917.2:n.466_466+1delinsGT
XR_002958634.1:n.466_466+1delinsGT
NM_000071.3:c.316_316+1delinsGT
NM_001178009.3:c.316_316+1delinsGT
NM_001178008.3:c.316_316+1delinsGT
NM_001320298.2:c.316_316+1delinsGT