Canonical Allele Identifier: CA2579804126
Gene: CBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43063019_43063021delinsAGC , CM000683.2:g.43063019_43063021delinsAGC GRCh38
NG_008938.1:g.17910_17912delinsGCT , LRG_777:g.17910_17912delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000398165.8:c.886_888delinsGCT MANE Select ENSP00000381231.4:p.Thr296Ala
ENST00000352178.9:c.886_888delinsGCT ENSP00000344460.5:p.Thr296Ala
ENST00000359624.7:c.886_888delinsGCT ENSP00000352643.3:p.Thr296Ala
ENST00000398158.5:c.886_888delinsGCT ENSP00000381225.1:p.Thr296Ala
ENST00000398165.7:c.886_888delinsGCT ENSP00000381231.3:p.Thr296Ala
ENST00000461686.5:n.1197_1199delinsGCT
ENST00000486098.1:n.228_230delinsGCT
ENST00000496485.1:n.386_388delinsGCT
NM_000071.2:c.886_888delinsGCT , LRG_777t1:c.886_888delinsGCT NP_000062.1:p.Thr296Ala
NM_001178008.1:c.886_888delinsGCT NP_001171479.1:p.Thr296Ala
NM_001178009.1:c.886_888delinsGCT NP_001171480.1:p.Thr296Ala
XM_011529773.1:c.937_939delinsGCT XP_011528075.1:p.Thr313Ala
XM_011529774.1:c.937_939delinsGCT XP_011528076.1:p.Thr313Ala
XM_011529775.1:c.937_939delinsGCT XP_011528077.1:p.Thr313Ala
XM_011529776.1:c.937_939delinsGCT XP_011528078.1:p.Thr313Ala
XM_011529777.1:c.886_888delinsGCT XP_011528079.1:p.Thr296Ala
XM_011529778.1:c.886_888delinsGCT XP_011528080.1:p.Thr296Ala
XM_011529779.1:c.886_888delinsGCT XP_011528081.1:p.Thr296Ala
XM_011529781.1:c.886_888delinsGCT XP_011528083.1:p.Thr296Ala
XM_011529782.1:c.886_888delinsGCT XP_011528084.1:p.Thr296Ala
XM_011529783.1:c.571_573delinsGCT XP_011528085.1:p.Thr191Ala
XM_011529784.1:c.571_573delinsGCT XP_011528086.1:p.Thr191Ala
NM_001178008.2:c.886_888delinsGCT NP_001171479.1:p.Thr296Ala
NM_001178009.2:c.886_888delinsGCT NP_001171480.1:p.Thr296Ala
NM_001320298.1:c.886_888delinsGCT NP_001307227.1:p.Thr296Ala
NM_001321072.1:c.571_573delinsGCT NP_001308001.1:p.Thr191Ala
XM_011529774.2:c.937_939delinsGCT XP_011528076.1:p.Thr313Ala
XM_011529777.2:c.886_888delinsGCT XP_011528079.1:p.Thr296Ala
XM_011529783.2:c.571_573delinsGCT XP_011528085.1:p.Thr191Ala
XM_017028491.2:c.886_888delinsGCT XP_016883980.1:p.Thr296Ala
XM_024452136.1:c.937_939delinsGCT XP_024307904.1:p.Thr313Ala
XM_024452137.1:c.937_939delinsGCT XP_024307905.1:p.Thr313Ala
XM_024452138.1:c.571_573delinsGCT XP_024307906.1:p.Thr191Ala
XM_024452139.1:c.571_573delinsGCT XP_024307907.1:p.Thr191Ala
XM_024452140.1:c.571_573delinsGCT XP_024307908.1:p.Thr191Ala
XR_001754915.1:n.1257_1259delinsGCT
XR_001754916.2:n.1036_1038delinsGCT
XR_001754917.2:n.1036_1038delinsGCT
XR_002958634.1:n.1857_1859delinsGCT
NM_000071.3:c.886_888delinsGCT MANE Select NP_000062.1:p.Thr296Ala
NM_001178009.3:c.886_888delinsGCT NP_001171480.1:p.Thr296Ala
NM_001178008.3:c.886_888delinsGCT NP_001171479.1:p.Thr296Ala
NM_001320298.2:c.886_888delinsGCT NP_001307227.1:p.Thr296Ala