Canonical Allele Identifier: CA2579805296

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43056855_43056857delinsGGT , CM000683.2:g.43056855_43056857delinsGGT	GRCh38
NG_008938.1:g.24074_24076delinsACC , LRG_777:g.24074_24076delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.1498_1500delinsACC MANE Select	ENSP00000381231.4:p.Ser500Thr
ENST00000352178.9:c.1498_1500delinsACC	ENSP00000344460.5:p.Ser500Thr
ENST00000359624.7:c.1498_1500delinsACC	ENSP00000352643.3:p.Ser500Thr
ENST00000398158.5:c.1498_1500delinsACC	ENSP00000381225.1:p.Ser500Thr
ENST00000398165.7:c.1498_1500delinsACC	ENSP00000381231.3:p.Ser500Thr
ENST00000430013.1:c.459_461delinsACC
ENST00000451248.5:c.248_250delinsACC
ENST00000458223.5:c.261_263delinsACC
ENST00000461686.5:n.1809_1811delinsACC
ENST00000462349.5:n.789_791delinsACC
ENST00000491776.1:n.433_435delinsACC
NM_000071.2:c.1498_1500delinsACC , LRG_777t1:c.1498_1500delinsACC	NP_000062.1:p.Ser500Thr
NM_001178008.1:c.1498_1500delinsACC	NP_001171479.1:p.Ser500Thr
NM_001178009.1:c.1498_1500delinsACC	NP_001171480.1:p.Ser500Thr
XM_011529773.1:c.1549_1551delinsACC	XP_011528075.1:p.Ser517Thr
XM_011529774.1:c.1549_1551delinsACC	XP_011528076.1:p.Ser517Thr
XM_011529775.1:c.1549_1551delinsACC	XP_011528077.1:p.Ser517Thr
XM_011529776.1:c.1549_1551delinsACC	XP_011528078.1:p.Ser517Thr
XM_011529777.1:c.1498_1500delinsACC	XP_011528079.1:p.Ser500Thr
XM_011529778.1:c.1498_1500delinsACC	XP_011528080.1:p.Ser500Thr
XM_011529779.1:c.1498_1500delinsACC	XP_011528081.1:p.Ser500Thr
XM_011529781.1:c.1498_1500delinsACC	XP_011528083.1:p.Ser500Thr
XM_011529782.1:c.1498_1500delinsACC	XP_011528084.1:p.Ser500Thr
XM_011529783.1:c.1183_1185delinsACC	XP_011528085.1:p.Ser395Thr
XM_011529784.1:c.1183_1185delinsACC	XP_011528086.1:p.Ser395Thr
NM_001178008.2:c.1498_1500delinsACC	NP_001171479.1:p.Ser500Thr
NM_001178009.2:c.1498_1500delinsACC	NP_001171480.1:p.Ser500Thr
NM_001320298.1:c.1498_1500delinsACC	NP_001307227.1:p.Ser500Thr
NM_001321072.1:c.1183_1185delinsACC	NP_001308001.1:p.Ser395Thr
XM_011529774.2:c.1549_1551delinsACC	XP_011528076.1:p.Ser517Thr
XM_011529777.2:c.1498_1500delinsACC	XP_011528079.1:p.Ser500Thr
XM_011529783.2:c.1183_1185delinsACC	XP_011528085.1:p.Ser395Thr
XM_017028491.2:c.1498_1500delinsACC	XP_016883980.1:p.Ser500Thr
XM_024452136.1:c.1549_1551delinsACC	XP_024307904.1:p.Ser517Thr
XM_024452137.1:c.1549_1551delinsACC	XP_024307905.1:p.Ser517Thr
XM_024452138.1:c.1183_1185delinsACC	XP_024307906.1:p.Ser395Thr
XM_024452139.1:c.1183_1185delinsACC	XP_024307907.1:p.Ser395Thr
XM_024452140.1:c.1183_1185delinsACC	XP_024307908.1:p.Ser395Thr
XR_001754915.1:n.1877_1879delinsACC
XR_001754916.2:n.1802_1804delinsACC
XR_001754917.2:n.1802_1804delinsACC
XR_002958634.1:n.2477_2479delinsACC
NM_000071.3:c.1498_1500delinsACC MANE Select	NP_000062.1:p.Ser500Thr
NM_001178009.3:c.1498_1500delinsACC	NP_001171480.1:p.Ser500Thr
NM_001178008.3:c.1498_1500delinsACC	NP_001171479.1:p.Ser500Thr
NM_001320298.2:c.1498_1500delinsACC	NP_001307227.1:p.Ser500Thr