Canonical Allele Identifier: CA2579812192
Gene: CBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43066319_43066320delinsAG , CM000683.2:g.43066319_43066320delinsAG GRCh38
NG_008938.1:g.14611_14612delinsCT , LRG_777:g.14611_14612delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000398165.8:c.374_375delinsCT MANE Select ENSP00000381231.4:p.Arg125Pro
ENST00000352178.9:c.374_375delinsCT ENSP00000344460.5:p.Arg125Pro
ENST00000359624.7:c.374_375delinsCT ENSP00000352643.3:p.Arg125Pro
ENST00000398158.5:c.374_375delinsCT ENSP00000381225.1:p.Arg125Pro
ENST00000398165.7:c.374_375delinsCT ENSP00000381231.3:p.Arg125Pro
ENST00000441030.5:c.374_375delinsCT ENSP00000388235.1:p.Arg125Pro
ENST00000461686.5:n.685_686delinsCT
ENST00000470912.5:n.817_818delinsCT
NM_000071.2:c.374_375delinsCT , LRG_777t1:c.374_375delinsCT NP_000062.1:p.Arg125Pro
NM_001178008.1:c.374_375delinsCT NP_001171479.1:p.Arg125Pro
NM_001178009.1:c.374_375delinsCT NP_001171480.1:p.Arg125Pro
XM_011529773.1:c.425_426delinsCT XP_011528075.1:p.Arg142Pro
XM_011529774.1:c.425_426delinsCT XP_011528076.1:p.Arg142Pro
XM_011529775.1:c.425_426delinsCT XP_011528077.1:p.Arg142Pro
XM_011529776.1:c.425_426delinsCT XP_011528078.1:p.Arg142Pro
XM_011529777.1:c.374_375delinsCT XP_011528079.1:p.Arg125Pro
XM_011529778.1:c.374_375delinsCT XP_011528080.1:p.Arg125Pro
XM_011529779.1:c.374_375delinsCT XP_011528081.1:p.Arg125Pro
XM_011529781.1:c.374_375delinsCT XP_011528083.1:p.Arg125Pro
XM_011529782.1:c.374_375delinsCT XP_011528084.1:p.Arg125Pro
XM_011529783.1:c.59_60delinsCT XP_011528085.1:p.Arg20Pro
XM_011529784.1:c.59_60delinsCT XP_011528086.1:p.Arg20Pro
NM_001178008.2:c.374_375delinsCT NP_001171479.1:p.Arg125Pro
NM_001178009.2:c.374_375delinsCT NP_001171480.1:p.Arg125Pro
NM_001320298.1:c.374_375delinsCT NP_001307227.1:p.Arg125Pro
NM_001321072.1:c.59_60delinsCT NP_001308001.1:p.Arg20Pro
XM_011529774.2:c.425_426delinsCT XP_011528076.1:p.Arg142Pro
XM_011529777.2:c.374_375delinsCT XP_011528079.1:p.Arg125Pro
XM_011529783.2:c.59_60delinsCT XP_011528085.1:p.Arg20Pro
XM_017028491.2:c.374_375delinsCT XP_016883980.1:p.Arg125Pro
XM_024452136.1:c.425_426delinsCT XP_024307904.1:p.Arg142Pro
XM_024452137.1:c.425_426delinsCT XP_024307905.1:p.Arg142Pro
XM_024452138.1:c.59_60delinsCT XP_024307906.1:p.Arg20Pro
XM_024452139.1:c.59_60delinsCT XP_024307907.1:p.Arg20Pro
XM_024452140.1:c.59_60delinsCT XP_024307908.1:p.Arg20Pro
XR_001754915.1:n.745_746delinsCT
XR_001754916.2:n.524_525delinsCT
XR_001754917.2:n.524_525delinsCT
XR_002958634.1:n.524_525delinsCT
NM_000071.3:c.374_375delinsCT MANE Select NP_000062.1:p.Arg125Pro
NM_001178009.3:c.374_375delinsCT NP_001171480.1:p.Arg125Pro
NM_001178008.3:c.374_375delinsCT NP_001171479.1:p.Arg125Pro
NM_001320298.2:c.374_375delinsCT NP_001307227.1:p.Arg125Pro