Canonical Allele Identifier: CA3796218

Gene: MOCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39913767G>A , CM000668.2:g.39913767G>A	GRCh38
NC_000006.11:g.39881511G>A , CM000668.1:g.39881511G>A	GRCh37
NC_000006.10:g.39989489G>A	NCBI36
NG_009297.1:g.25744C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001358530.2:c.645+7C>T MANE Select	NP_001345459.1:n.645+7C>T
ENST00000340692.10:c.645+7C>T MANE Select	ENSP00000344794.5:n.645+7C>T
NM_001075098.3:c.645+7C>T	NP_001068566.1:n.645+7C>T
NM_001075098.4:c.645+7C>T	NP_001068566.1:n.645+7C>T
NM_001358529.1:c.645+7C>T	NP_001345458.1:n.645+7C>T
NM_001358529.2:c.645+7C>T	NP_001345458.1:n.645+7C>T
NM_001358530.1:c.645+7C>T	NP_001345459.1:n.645+7C>T
NM_001358531.1:c.384+7C>T	NP_001345460.1:n.384+7C>T
NM_001358531.2:c.384+7C>T	NP_001345460.1:n.384+7C>T
NM_001358533.1:c.384+7C>T	NP_001345462.1:n.384+7C>T
NM_001358533.2:c.384+7C>T	NP_001345462.1:n.384+7C>T
NM_001358534.1:c.384+7C>T	NP_001345463.1:n.384+7C>T
NM_001358534.2:c.384+7C>T	NP_001345463.1:n.384+7C>T
NM_005943.5:c.645+7C>T	NP_005934.2:n.645+7C>T
NM_005943.6:c.645+7C>T	NP_005934.2:n.645+7C>T
NR_033233.1:n.652+7C>T
NR_033233.2:n.563+7C>T
ENST00000340692.9:c.645+7C>T	ENSP00000344794.5:n.645+7C>T
ENST00000373181.8:c.384+7C>T	ENSP00000362277.4:n.384+7C>T
ENST00000373186.8:c.645+7C>T	ENSP00000362282.4:n.645+7C>T
ENST00000373188.6:c.645+7C>T	ENSP00000362284.2:n.645+7C>T
ENST00000373195.7:c.384+7C>T	ENSP00000362291.3:n.384+7C>T
ENST00000425303.6:c.645+7C>T	ENSP00000416478.2:n.645+7C>T
ENST00000432280.2:c.558+7C>T	ENSP00000410809.2:n.558+7C>T
ENST00000473742.1:n.532C>T
ENST00000645522.1:n.783+7C>T
XM_011514632.1:c.645+7C>T	XP_011512934.1:n.645+7C>T
XM_011514633.1:c.645+7C>T	XP_011512935.1:n.645+7C>T
XM_011514634.1:c.384+7C>T	XP_011512936.1:n.384+7C>T
XM_011514635.1:c.645+7C>T	XP_011512937.1:n.645+7C>T
XR_926225.1:n.690+7C>T