Canonical Allele Identifier: CA2579811083

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43056837_43056839delinsCGA , CM000683.2:g.43056837_43056839delinsCGA	GRCh38
NG_008938.1:g.24092_24094delinsTCG , LRG_777:g.24092_24094delinsTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.1516_1518delinsTCG MANE Select	ENSP00000381231.4:p.Asp506Ser
ENST00000352178.9:c.1516_1518delinsTCG	ENSP00000344460.5:p.Asp506Ser
ENST00000359624.7:c.1516_1518delinsTCG	ENSP00000352643.3:p.Asp506Ser
ENST00000398158.5:c.1516_1518delinsTCG	ENSP00000381225.1:p.Asp506Ser
ENST00000398165.7:c.1516_1518delinsTCG	ENSP00000381231.3:p.Asp506Ser
ENST00000430013.1:c.477_479delinsTCG
ENST00000451248.5:c.266_268delinsTCG
ENST00000458223.5:c.279_281delinsTCG
ENST00000461686.5:n.1827_1829delinsTCG
ENST00000462349.5:n.807_809delinsTCG
ENST00000491776.1:n.451_453delinsTCG
NM_000071.2:c.1516_1518delinsTCG , LRG_777t1:c.1516_1518delinsTCG	NP_000062.1:p.Asp506Ser
NM_001178008.1:c.1516_1518delinsTCG	NP_001171479.1:p.Asp506Ser
NM_001178009.1:c.1516_1518delinsTCG	NP_001171480.1:p.Asp506Ser
XM_011529773.1:c.1567_1569delinsTCG	XP_011528075.1:p.Asp523Ser
XM_011529774.1:c.1567_1569delinsTCG	XP_011528076.1:p.Asp523Ser
XM_011529775.1:c.1567_1569delinsTCG	XP_011528077.1:p.Asp523Ser
XM_011529776.1:c.1567_1569delinsTCG	XP_011528078.1:p.Asp523Ser
XM_011529777.1:c.1516_1518delinsTCG	XP_011528079.1:p.Asp506Ser
XM_011529778.1:c.1516_1518delinsTCG	XP_011528080.1:p.Asp506Ser
XM_011529779.1:c.1516_1518delinsTCG	XP_011528081.1:p.Asp506Ser
XM_011529781.1:c.1516_1518delinsTCG	XP_011528083.1:p.Asp506Ser
XM_011529782.1:c.1516_1518delinsTCG	XP_011528084.1:p.Asp506Ser
XM_011529783.1:c.1201_1203delinsTCG	XP_011528085.1:p.Asp401Ser
XM_011529784.1:c.1201_1203delinsTCG	XP_011528086.1:p.Asp401Ser
NM_001178008.2:c.1516_1518delinsTCG	NP_001171479.1:p.Asp506Ser
NM_001178009.2:c.1516_1518delinsTCG	NP_001171480.1:p.Asp506Ser
NM_001320298.1:c.1516_1518delinsTCG	NP_001307227.1:p.Asp506Ser
NM_001321072.1:c.1201_1203delinsTCG	NP_001308001.1:p.Asp401Ser
XM_011529774.2:c.1567_1569delinsTCG	XP_011528076.1:p.Asp523Ser
XM_011529777.2:c.1516_1518delinsTCG	XP_011528079.1:p.Asp506Ser
XM_011529783.2:c.1201_1203delinsTCG	XP_011528085.1:p.Asp401Ser
XM_017028491.2:c.1516_1518delinsTCG	XP_016883980.1:p.Asp506Ser
XM_024452136.1:c.1567_1569delinsTCG	XP_024307904.1:p.Asp523Ser
XM_024452137.1:c.1567_1569delinsTCG	XP_024307905.1:p.Asp523Ser
XM_024452138.1:c.1201_1203delinsTCG	XP_024307906.1:p.Asp401Ser
XM_024452139.1:c.1201_1203delinsTCG	XP_024307907.1:p.Asp401Ser
XM_024452140.1:c.1201_1203delinsTCG	XP_024307908.1:p.Asp401Ser
XR_001754915.1:n.1895_1897delinsTCG
XR_001754916.2:n.1820_1822delinsTCG
XR_001754917.2:n.1820_1822delinsTCG
XR_002958634.1:n.2495_2497delinsTCG
NM_000071.3:c.1516_1518delinsTCG MANE Select	NP_000062.1:p.Asp506Ser
NM_001178009.3:c.1516_1518delinsTCG	NP_001171480.1:p.Asp506Ser
NM_001178008.3:c.1516_1518delinsTCG	NP_001171479.1:p.Asp506Ser
NM_001320298.2:c.1516_1518delinsTCG	NP_001307227.1:p.Asp506Ser