Canonical Allele Identifier: CA2579805065
Gene: CBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43063052_43063054delinsCTG , CM000683.2:g.43063052_43063054delinsCTG GRCh38
NG_008938.1:g.17877_17879delinsCAG , LRG_777:g.17877_17879delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000398165.8:c.853_855delinsCAG MANE Select ENSP00000381231.4:p.Ser285Gln
ENST00000352178.9:c.853_855delinsCAG ENSP00000344460.5:p.Ser285Gln
ENST00000359624.7:c.853_855delinsCAG ENSP00000352643.3:p.Ser285Gln
ENST00000398158.5:c.853_855delinsCAG ENSP00000381225.1:p.Ser285Gln
ENST00000398165.7:c.853_855delinsCAG ENSP00000381231.3:p.Ser285Gln
ENST00000461686.5:n.1164_1166delinsCAG
ENST00000486098.1:n.195_197delinsCAG
ENST00000496485.1:n.353_355delinsCAG
NM_000071.2:c.853_855delinsCAG , LRG_777t1:c.853_855delinsCAG NP_000062.1:p.Ser285Gln
NM_001178008.1:c.853_855delinsCAG NP_001171479.1:p.Ser285Gln
NM_001178009.1:c.853_855delinsCAG NP_001171480.1:p.Ser285Gln
XM_011529773.1:c.904_906delinsCAG XP_011528075.1:p.Ser302Gln
XM_011529774.1:c.904_906delinsCAG XP_011528076.1:p.Ser302Gln
XM_011529775.1:c.904_906delinsCAG XP_011528077.1:p.Ser302Gln
XM_011529776.1:c.904_906delinsCAG XP_011528078.1:p.Ser302Gln
XM_011529777.1:c.853_855delinsCAG XP_011528079.1:p.Ser285Gln
XM_011529778.1:c.853_855delinsCAG XP_011528080.1:p.Ser285Gln
XM_011529779.1:c.853_855delinsCAG XP_011528081.1:p.Ser285Gln
XM_011529781.1:c.853_855delinsCAG XP_011528083.1:p.Ser285Gln
XM_011529782.1:c.853_855delinsCAG XP_011528084.1:p.Ser285Gln
XM_011529783.1:c.538_540delinsCAG XP_011528085.1:p.Ser180Gln
XM_011529784.1:c.538_540delinsCAG XP_011528086.1:p.Ser180Gln
NM_001178008.2:c.853_855delinsCAG NP_001171479.1:p.Ser285Gln
NM_001178009.2:c.853_855delinsCAG NP_001171480.1:p.Ser285Gln
NM_001320298.1:c.853_855delinsCAG NP_001307227.1:p.Ser285Gln
NM_001321072.1:c.538_540delinsCAG NP_001308001.1:p.Ser180Gln
XM_011529774.2:c.904_906delinsCAG XP_011528076.1:p.Ser302Gln
XM_011529777.2:c.853_855delinsCAG XP_011528079.1:p.Ser285Gln
XM_011529783.2:c.538_540delinsCAG XP_011528085.1:p.Ser180Gln
XM_017028491.2:c.853_855delinsCAG XP_016883980.1:p.Ser285Gln
XM_024452136.1:c.904_906delinsCAG XP_024307904.1:p.Ser302Gln
XM_024452137.1:c.904_906delinsCAG XP_024307905.1:p.Ser302Gln
XM_024452138.1:c.538_540delinsCAG XP_024307906.1:p.Ser180Gln
XM_024452139.1:c.538_540delinsCAG XP_024307907.1:p.Ser180Gln
XM_024452140.1:c.538_540delinsCAG XP_024307908.1:p.Ser180Gln
XR_001754915.1:n.1224_1226delinsCAG
XR_001754916.2:n.1003_1005delinsCAG
XR_001754917.2:n.1003_1005delinsCAG
XR_002958634.1:n.1824_1826delinsCAG
NM_000071.3:c.853_855delinsCAG MANE Select NP_000062.1:p.Ser285Gln
NM_001178009.3:c.853_855delinsCAG NP_001171480.1:p.Ser285Gln
NM_001178008.3:c.853_855delinsCAG NP_001171479.1:p.Ser285Gln
NM_001320298.2:c.853_855delinsCAG NP_001307227.1:p.Ser285Gln