Canonical Allele Identifier: CA2573054941

Gene: CBS

Linked Data

• ClinVar Variation Id: 1180849
• ClinVar RCV Id: RCV001814578
• dbSNP Id: rs2146394968

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43066327_43066336del , CM000683.2:g.43066327_43066336del	GRCh38
NG_008938.1:g.14596_14605del , LRG_777:g.14596_14605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.359_368del MANE Select	ENSP00000381231.4:p.Asp120AlafsTer4
ENST00000352178.9:c.359_368del	ENSP00000344460.5:p.Asp120AlafsTer4
ENST00000359624.7:c.359_368del	ENSP00000352643.3:p.Asp120AlafsTer4
ENST00000398158.5:c.359_368del	ENSP00000381225.1:p.Asp120AlafsTer4
ENST00000398165.7:c.359_368del	ENSP00000381231.3:p.Asp120AlafsTer4
ENST00000441030.5:c.359_368del	ENSP00000388235.1:p.Asp120AlafsTer4
ENST00000461686.5:n.670_679del
ENST00000470912.5:n.802_811del
NM_000071.2:c.359_368del , LRG_777t1:c.359_368del	NP_000062.1:p.Asp120AlafsTer4
NM_001178008.1:c.359_368del	NP_001171479.1:p.Asp120AlafsTer4
NM_001178009.1:c.359_368del	NP_001171480.1:p.Asp120AlafsTer4
XM_011529773.1:c.410_419del	XP_011528075.1:p.Asp137AlafsTer4
XM_011529774.1:c.410_419del	XP_011528076.1:p.Asp137AlafsTer4
XM_011529775.1:c.410_419del	XP_011528077.1:p.Asp137AlafsTer4
XM_011529776.1:c.410_419del	XP_011528078.1:p.Asp137AlafsTer4
XM_011529777.1:c.359_368del	XP_011528079.1:p.Asp120AlafsTer4
XM_011529778.1:c.359_368del	XP_011528080.1:p.Asp120AlafsTer4
XM_011529779.1:c.359_368del	XP_011528081.1:p.Asp120AlafsTer4
XM_011529781.1:c.359_368del	XP_011528083.1:p.Asp120AlafsTer4
XM_011529782.1:c.359_368del	XP_011528084.1:p.Asp120AlafsTer4
XM_011529783.1:c.44_53del	XP_011528085.1:p.Asp15AlafsTer4
XM_011529784.1:c.44_53del	XP_011528086.1:p.Asp15AlafsTer4
NM_001178008.2:c.359_368del	NP_001171479.1:p.Asp120AlafsTer4
NM_001178009.2:c.359_368del	NP_001171480.1:p.Asp120AlafsTer4
NM_001320298.1:c.359_368del	NP_001307227.1:p.Asp120AlafsTer4
NM_001321072.1:c.44_53del	NP_001308001.1:p.Asp15AlafsTer4
XM_011529774.2:c.410_419del	XP_011528076.1:p.Asp137AlafsTer4
XM_011529777.2:c.359_368del	XP_011528079.1:p.Asp120AlafsTer4
XM_011529783.2:c.44_53del	XP_011528085.1:p.Asp15AlafsTer4
XM_017028491.2:c.359_368del	XP_016883980.1:p.Asp120AlafsTer4
XM_024452136.1:c.410_419del	XP_024307904.1:p.Asp137AlafsTer4
XM_024452137.1:c.410_419del	XP_024307905.1:p.Asp137AlafsTer4
XM_024452138.1:c.44_53del	XP_024307906.1:p.Asp15AlafsTer4
XM_024452139.1:c.44_53del	XP_024307907.1:p.Asp15AlafsTer4
XM_024452140.1:c.44_53del	XP_024307908.1:p.Asp15AlafsTer4
XR_001754915.1:n.730_739del
XR_001754916.2:n.509_518del
XR_001754917.2:n.509_518del
XR_002958634.1:n.509_518del
NM_000071.3:c.359_368del MANE Select	NP_000062.1:p.Asp120AlafsTer4
NM_001178009.3:c.359_368del	NP_001171480.1:p.Asp120AlafsTer4
NM_001178008.3:c.359_368del	NP_001171479.1:p.Asp120AlafsTer4
NM_001320298.2:c.359_368del	NP_001307227.1:p.Asp120AlafsTer4