Canonical Allele Identifier: CA2579807120

Gene: CBS

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43056879_43056881delinsACT , CM000683.2:g.43056879_43056881delinsACT	GRCh38
NG_008938.1:g.24050_24052delinsAGT , LRG_777:g.24050_24052delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.1474_1476delinsAGT MANE Select	ENSP00000381231.4:p.Leu492Ser
ENST00000352178.9:c.1474_1476delinsAGT	ENSP00000344460.5:p.Leu492Ser
ENST00000359624.7:c.1474_1476delinsAGT	ENSP00000352643.3:p.Leu492Ser
ENST00000398158.5:c.1474_1476delinsAGT	ENSP00000381225.1:p.Leu492Ser
ENST00000398165.7:c.1474_1476delinsAGT	ENSP00000381231.3:p.Leu492Ser
ENST00000430013.1:c.435_437delinsAGT
ENST00000451248.5:c.224_226delinsAGT
ENST00000458223.5:c.237_239delinsAGT
ENST00000461686.5:n.1785_1787delinsAGT
ENST00000462349.5:n.765_767delinsAGT
ENST00000491776.1:n.409_411delinsAGT
NM_000071.2:c.1474_1476delinsAGT , LRG_777t1:c.1474_1476delinsAGT	NP_000062.1:p.Leu492Ser
NM_001178008.1:c.1474_1476delinsAGT	NP_001171479.1:p.Leu492Ser
NM_001178009.1:c.1474_1476delinsAGT	NP_001171480.1:p.Leu492Ser
XM_011529773.1:c.1525_1527delinsAGT	XP_011528075.1:p.Leu509Ser
XM_011529774.1:c.1525_1527delinsAGT	XP_011528076.1:p.Leu509Ser
XM_011529775.1:c.1525_1527delinsAGT	XP_011528077.1:p.Leu509Ser
XM_011529776.1:c.1525_1527delinsAGT	XP_011528078.1:p.Leu509Ser
XM_011529777.1:c.1474_1476delinsAGT	XP_011528079.1:p.Leu492Ser
XM_011529778.1:c.1474_1476delinsAGT	XP_011528080.1:p.Leu492Ser
XM_011529779.1:c.1474_1476delinsAGT	XP_011528081.1:p.Leu492Ser
XM_011529781.1:c.1474_1476delinsAGT	XP_011528083.1:p.Leu492Ser
XM_011529782.1:c.1474_1476delinsAGT	XP_011528084.1:p.Leu492Ser
XM_011529783.1:c.1159_1161delinsAGT	XP_011528085.1:p.Leu387Ser
XM_011529784.1:c.1159_1161delinsAGT	XP_011528086.1:p.Leu387Ser
NM_001178008.2:c.1474_1476delinsAGT	NP_001171479.1:p.Leu492Ser
NM_001178009.2:c.1474_1476delinsAGT	NP_001171480.1:p.Leu492Ser
NM_001320298.1:c.1474_1476delinsAGT	NP_001307227.1:p.Leu492Ser
NM_001321072.1:c.1159_1161delinsAGT	NP_001308001.1:p.Leu387Ser
XM_011529774.2:c.1525_1527delinsAGT	XP_011528076.1:p.Leu509Ser
XM_011529777.2:c.1474_1476delinsAGT	XP_011528079.1:p.Leu492Ser
XM_011529783.2:c.1159_1161delinsAGT	XP_011528085.1:p.Leu387Ser
XM_017028491.2:c.1474_1476delinsAGT	XP_016883980.1:p.Leu492Ser
XM_024452136.1:c.1525_1527delinsAGT	XP_024307904.1:p.Leu509Ser
XM_024452137.1:c.1525_1527delinsAGT	XP_024307905.1:p.Leu509Ser
XM_024452138.1:c.1159_1161delinsAGT	XP_024307906.1:p.Leu387Ser
XM_024452139.1:c.1159_1161delinsAGT	XP_024307907.1:p.Leu387Ser
XM_024452140.1:c.1159_1161delinsAGT	XP_024307908.1:p.Leu387Ser
XR_001754915.1:n.1853_1855delinsAGT
XR_001754916.2:n.1778_1780delinsAGT
XR_001754917.2:n.1778_1780delinsAGT
XR_002958634.1:n.2453_2455delinsAGT
NM_000071.3:c.1474_1476delinsAGT MANE Select	NP_000062.1:p.Leu492Ser
NM_001178009.3:c.1474_1476delinsAGT	NP_001171480.1:p.Leu492Ser
NM_001178008.3:c.1474_1476delinsAGT	NP_001171479.1:p.Leu492Ser
NM_001320298.2:c.1474_1476delinsAGT	NP_001307227.1:p.Leu492Ser