Canonical Allele Identifier: CA3796263

Gene: MOCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39916167G>A , CM000668.2:g.39916167G>A	GRCh38
NC_000006.11:g.39883911G>A , CM000668.1:g.39883911G>A	GRCh37
NC_000006.10:g.39991889G>A	NCBI36
NG_009297.1:g.23344C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001358530.2:c.484C>T MANE Select	NP_001345459.1:p.Arg162Trp
ENST00000340692.10:c.484C>T MANE Select	ENSP00000344794.5:p.Arg162Trp
NM_001075098.3:c.484C>T	NP_001068566.1:p.Arg162Trp
NM_001075098.4:c.484C>T	NP_001068566.1:p.Arg162Trp
NM_001358529.1:c.484C>T	NP_001345458.1:p.Arg162Trp
NM_001358529.2:c.484C>T	NP_001345458.1:p.Arg162Trp
NM_001358530.1:c.484C>T	NP_001345459.1:p.Arg162Trp
NM_001358531.1:c.223C>T	NP_001345460.1:p.Arg75Trp
NM_001358531.2:c.223C>T	NP_001345460.1:p.Arg75Trp
NM_001358533.1:c.223C>T	NP_001345462.1:p.Arg75Trp
NM_001358533.2:c.223C>T	NP_001345462.1:p.Arg75Trp
NM_001358534.1:c.223C>T	NP_001345463.1:p.Arg75Trp
NM_001358534.2:c.223C>T	NP_001345463.1:p.Arg75Trp
NM_005943.5:c.484C>T	NP_005934.2:p.Arg162Trp
NM_005943.6:c.484C>T	NP_005934.2:p.Arg162Trp
NR_033233.1:n.491C>T
NR_033233.2:n.402C>T
ENST00000340692.9:c.484C>T	ENSP00000344794.5:p.Arg162Trp
ENST00000373181.8:c.223C>T	ENSP00000362277.4:p.Arg75Trp
ENST00000373186.8:c.484C>T	ENSP00000362282.4:p.Arg162Trp
ENST00000373188.6:c.484C>T	ENSP00000362284.2:p.Arg162Trp
ENST00000373195.7:c.223C>T	ENSP00000362291.3:p.Arg75Trp
ENST00000425303.6:c.484C>T	ENSP00000416478.2:p.Arg162Trp
ENST00000432280.2:c.397C>T	ENSP00000410809.2:p.Arg133Trp
ENST00000473742.1:n.364C>T
ENST00000645522.1:n.622C>T
XM_011514632.1:c.484C>T	XP_011512934.1:p.Arg162Trp
XM_011514633.1:c.484C>T	XP_011512935.1:p.Arg162Trp
XM_011514634.1:c.223C>T	XP_011512936.1:p.Arg75Trp
XM_011514635.1:c.484C>T	XP_011512937.1:p.Arg162Trp
XR_926225.1:n.529C>T