Canonical Allele Identifier: CA2579805169

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43058911_43058913delinsAGA , CM000683.2:g.43058911_43058913delinsAGA	GRCh38
NG_008938.1:g.22018_22020delinsTCT , LRG_777:g.22018_22020delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.1279_1281delinsTCT MANE Select	ENSP00000381231.4:p.Pro427Ser
ENST00000352178.9:c.1279_1281delinsTCT	ENSP00000344460.5:p.Pro427Ser
ENST00000359624.7:c.1279_1281delinsTCT	ENSP00000352643.3:p.Pro427Ser
ENST00000398158.5:c.1279_1281delinsTCT	ENSP00000381225.1:p.Pro427Ser
ENST00000398165.7:c.1279_1281delinsTCT	ENSP00000381231.3:p.Pro427Ser
ENST00000430013.1:c.240_242delinsTCT
ENST00000451248.5:c.29_31delinsTCT
ENST00000458223.5:c.42_44delinsTCT
ENST00000461686.5:n.1590_1592delinsTCT
ENST00000462349.5:n.570_572delinsTCT
ENST00000491776.1:n.214_216delinsTCT
NM_000071.2:c.1279_1281delinsTCT , LRG_777t1:c.1279_1281delinsTCT	NP_000062.1:p.Pro427Ser
NM_001178008.1:c.1279_1281delinsTCT	NP_001171479.1:p.Pro427Ser
NM_001178009.1:c.1279_1281delinsTCT	NP_001171480.1:p.Pro427Ser
XM_011529773.1:c.1330_1332delinsTCT	XP_011528075.1:p.Pro444Ser
XM_011529774.1:c.1330_1332delinsTCT	XP_011528076.1:p.Pro444Ser
XM_011529775.1:c.1330_1332delinsTCT	XP_011528077.1:p.Pro444Ser
XM_011529776.1:c.1330_1332delinsTCT	XP_011528078.1:p.Pro444Ser
XM_011529777.1:c.1279_1281delinsTCT	XP_011528079.1:p.Pro427Ser
XM_011529778.1:c.1279_1281delinsTCT	XP_011528080.1:p.Pro427Ser
XM_011529779.1:c.1279_1281delinsTCT	XP_011528081.1:p.Pro427Ser
XM_011529781.1:c.1279_1281delinsTCT	XP_011528083.1:p.Pro427Ser
XM_011529782.1:c.1279_1281delinsTCT	XP_011528084.1:p.Pro427Ser
XM_011529783.1:c.964_966delinsTCT	XP_011528085.1:p.Pro322Ser
XM_011529784.1:c.964_966delinsTCT	XP_011528086.1:p.Pro322Ser
NM_001178008.2:c.1279_1281delinsTCT	NP_001171479.1:p.Pro427Ser
NM_001178009.2:c.1279_1281delinsTCT	NP_001171480.1:p.Pro427Ser
NM_001320298.1:c.1279_1281delinsTCT	NP_001307227.1:p.Pro427Ser
NM_001321072.1:c.964_966delinsTCT	NP_001308001.1:p.Pro322Ser
XM_011529774.2:c.1330_1332delinsTCT	XP_011528076.1:p.Pro444Ser
XM_011529777.2:c.1279_1281delinsTCT	XP_011528079.1:p.Pro427Ser
XM_011529783.2:c.964_966delinsTCT	XP_011528085.1:p.Pro322Ser
XM_017028491.2:c.1279_1281delinsTCT	XP_016883980.1:p.Pro427Ser
XM_024452136.1:c.1330_1332delinsTCT	XP_024307904.1:p.Pro444Ser
XM_024452137.1:c.1330_1332delinsTCT	XP_024307905.1:p.Pro444Ser
XM_024452138.1:c.964_966delinsTCT	XP_024307906.1:p.Pro322Ser
XM_024452139.1:c.964_966delinsTCT	XP_024307907.1:p.Pro322Ser
XM_024452140.1:c.964_966delinsTCT	XP_024307908.1:p.Pro322Ser
XR_001754915.1:n.1650_1652delinsTCT
XR_001754916.2:n.1429_1431delinsTCT
XR_001754917.2:n.1429_1431delinsTCT
XR_002958634.1:n.2250_2252delinsTCT
NM_000071.3:c.1279_1281delinsTCT MANE Select	NP_000062.1:p.Pro427Ser
NM_001178009.3:c.1279_1281delinsTCT	NP_001171480.1:p.Pro427Ser
NM_001178008.3:c.1279_1281delinsTCT	NP_001171479.1:p.Pro427Ser
NM_001320298.2:c.1279_1281delinsTCT	NP_001307227.1:p.Pro427Ser