Canonical Allele Identifier: CA2579812277

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43065417_43065418delinsAG , CM000683.2:g.43065417_43065418delinsAG	GRCh38
NG_008938.1:g.15513_15514delinsCT , LRG_777:g.15513_15514delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.635_636delinsCT MANE Select	ENSP00000381231.4:p.Asn212Thr
ENST00000352178.9:c.635_636delinsCT	ENSP00000344460.5:p.Asn212Thr
ENST00000359624.7:c.635_636delinsCT	ENSP00000352643.3:p.Asn212Thr
ENST00000398158.5:c.635_636delinsCT	ENSP00000381225.1:p.Asn212Thr
ENST00000398165.7:c.635_636delinsCT	ENSP00000381231.3:p.Asn212Thr
ENST00000461686.5:n.946_947delinsCT
NM_000071.2:c.635_636delinsCT , LRG_777t1:c.635_636delinsCT	NP_000062.1:p.Asn212Thr
NM_001178008.1:c.635_636delinsCT	NP_001171479.1:p.Asn212Thr
NM_001178009.1:c.635_636delinsCT	NP_001171480.1:p.Asn212Thr
XM_011529773.1:c.686_687delinsCT	XP_011528075.1:p.Asn229Thr
XM_011529774.1:c.686_687delinsCT	XP_011528076.1:p.Asn229Thr
XM_011529775.1:c.686_687delinsCT	XP_011528077.1:p.Asn229Thr
XM_011529776.1:c.686_687delinsCT	XP_011528078.1:p.Asn229Thr
XM_011529777.1:c.635_636delinsCT	XP_011528079.1:p.Asn212Thr
XM_011529778.1:c.635_636delinsCT	XP_011528080.1:p.Asn212Thr
XM_011529779.1:c.635_636delinsCT	XP_011528081.1:p.Asn212Thr
XM_011529781.1:c.635_636delinsCT	XP_011528083.1:p.Asn212Thr
XM_011529782.1:c.635_636delinsCT	XP_011528084.1:p.Asn212Thr
XM_011529783.1:c.320_321delinsCT	XP_011528085.1:p.Asn107Thr
XM_011529784.1:c.320_321delinsCT	XP_011528086.1:p.Asn107Thr
NM_001178008.2:c.635_636delinsCT	NP_001171479.1:p.Asn212Thr
NM_001178009.2:c.635_636delinsCT	NP_001171480.1:p.Asn212Thr
NM_001320298.1:c.635_636delinsCT	NP_001307227.1:p.Asn212Thr
NM_001321072.1:c.320_321delinsCT	NP_001308001.1:p.Asn107Thr
XM_011529774.2:c.686_687delinsCT	XP_011528076.1:p.Asn229Thr
XM_011529777.2:c.635_636delinsCT	XP_011528079.1:p.Asn212Thr
XM_011529783.2:c.320_321delinsCT	XP_011528085.1:p.Asn107Thr
XM_017028491.2:c.635_636delinsCT	XP_016883980.1:p.Asn212Thr
XM_024452136.1:c.686_687delinsCT	XP_024307904.1:p.Asn229Thr
XM_024452137.1:c.686_687delinsCT	XP_024307905.1:p.Asn229Thr
XM_024452138.1:c.320_321delinsCT	XP_024307906.1:p.Asn107Thr
XM_024452139.1:c.320_321delinsCT	XP_024307907.1:p.Asn107Thr
XM_024452140.1:c.320_321delinsCT	XP_024307908.1:p.Asn107Thr
XR_001754915.1:n.1006_1007delinsCT
XR_001754916.2:n.785_786delinsCT
XR_001754917.2:n.785_786delinsCT
XR_002958634.1:n.785_786delinsCT
NM_000071.3:c.635_636delinsCT MANE Select	NP_000062.1:p.Asn212Thr
NM_001178009.3:c.635_636delinsCT	NP_001171480.1:p.Asn212Thr
NM_001178008.3:c.635_636delinsCT	NP_001171479.1:p.Asn212Thr
NM_001320298.2:c.635_636delinsCT	NP_001307227.1:p.Asn212Thr