Canonical Allele Identifier: CA364041745

Gene: MOCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39909055C>A , CM000668.2:g.39909055C>A	GRCh38
NC_000006.11:g.39876831C>A , CM000668.1:g.39876831C>A	GRCh37
NC_000006.10:g.39984809C>A	NCBI36
NG_009297.1:g.30424G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001358530.2:c.1150G>T MANE Select	NP_001345459.1:p.Glu384Ter
ENST00000340692.10:c.1150G>T MANE Select	ENSP00000344794.5:p.Glu384Ter
NM_001075098.3:c.1150G>T	NP_001068566.1:p.Gly384Cys
NM_001075098.4:c.1150G>T	NP_001068566.1:p.Gly384Cys
NM_001358529.1:c.1102+780G>T	NP_001345458.1:n.1102+780G>T
NM_001358529.2:c.1102+780G>T	NP_001345458.1:n.1102+780G>T
NM_001358530.1:c.1150G>T	NP_001345459.1:p.Glu384Ter
NM_001358531.1:c.889G>T	NP_001345460.1:p.Glu297Ter
NM_001358531.2:c.889G>T	NP_001345460.1:p.Glu297Ter
NM_001358533.1:c.889G>T	NP_001345462.1:p.Gly297Cys
NM_001358533.2:c.889G>T	NP_001345462.1:p.Gly297Cys
NM_001358534.1:c.889G>T	NP_001345463.1:p.Gly297Cys
NM_001358534.2:c.889G>T	NP_001345463.1:p.Gly297Cys
NM_005943.5:c.1150G>T	NP_005934.2:p.Gly384Cys
NM_005943.6:c.1150G>T	NP_005934.2:p.Gly384Cys
NR_033233.1:n.1109+780G>T
NR_033233.2:n.1020+780G>T
ENST00000340692.9:c.1150G>T	ENSP00000344794.5:p.Glu384Ter
ENST00000373181.8:c.841+780G>T	ENSP00000362277.4:n.841+780G>T
ENST00000373186.8:c.1150G>T	ENSP00000362282.4:p.Gly384Cys
ENST00000373188.6:c.1150G>T	ENSP00000362284.2:p.Gly384Cys
ENST00000373195.7:c.841+780G>T	ENSP00000362291.3:n.841+780G>T
ENST00000425303.6:c.1150G>T	ENSP00000416478.2:p.Glu384Ter
ENST00000432280.2:c.1063G>T	ENSP00000410809.2:p.Gly355Cys
ENST00000645522.1:n.1288G>T
XM_011514632.1:c.1150G>T	XP_011512934.1:p.Glu384Ter
XM_011514633.1:c.1102+780G>T	XP_011512935.1:n.1102+780G>T
XM_011514634.1:c.889G>T	XP_011512936.1:p.Glu297Ter
XM_011514635.1:c.1150G>T	XP_011512937.1:p.Glu384Ter
XR_926225.1:n.1195G>T