Canonical Allele Identifier: CA1622892923

Gene: MOCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39912200A= , CM000668.2:g.39912200A=	GRCh38
NC_000006.11:g.39879944A= , CM000668.1:g.39879944A=	GRCh37
NC_000006.10:g.39987922A=	NCBI36
NG_009297.1:g.27311T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340692.10:c.981+64T= MANE Select	ENSP00000344794.5:n.981+64T=
ENST00000645522.1:n.1119+64T=
ENST00000340692.9:c.981+64T=	ENSP00000344794.5:n.981+64T=
ENST00000373181.8:c.720+64T=	ENSP00000362277.4:n.720+64T=
ENST00000373186.8:c.981+64T=	ENSP00000362282.4:n.981+64T=
ENST00000373188.6:c.981+64T=	ENSP00000362284.2:n.981+64T=
ENST00000373195.7:c.720+64T=	ENSP00000362291.3:n.720+64T=
ENST00000425303.6:c.981+64T=	ENSP00000416478.2:n.981+64T=
ENST00000432280.2:c.894+64T=	ENSP00000410809.2:n.894+64T=
NM_001075098.3:c.981+64T=	NP_001068566.1:n.981+64T=
NM_005943.5:c.981+64T=	NP_005934.2:n.981+64T=
NR_033233.1:n.988+64T=
XM_011514632.1:c.981+64T=	XP_011512934.1:n.981+64T=
XM_011514633.1:c.981+64T=	XP_011512935.1:n.981+64T=
XM_011514634.1:c.720+64T=	XP_011512936.1:n.720+64T=
XM_011514635.1:c.981+64T=	XP_011512937.1:n.981+64T=
XR_926225.1:n.1026+64T=
NM_001358529.1:c.981+64T=	NP_001345458.1:n.981+64T=
NM_001358530.1:c.981+64T=	NP_001345459.1:n.981+64T=
NM_001358531.1:c.720+64T=	NP_001345460.1:n.720+64T=
NM_001358533.1:c.720+64T=	NP_001345462.1:n.720+64T=
NM_001358534.1:c.720+64T=	NP_001345463.1:n.720+64T=
NM_001358530.2:c.981+64T= MANE Select	NP_001345459.1:n.981+64T=
NM_001075098.4:c.981+64T=	NP_001068566.1:n.981+64T=
NM_001358529.2:c.981+64T=	NP_001345458.1:n.981+64T=
NM_001358531.2:c.720+64T=	NP_001345460.1:n.720+64T=
NM_001358533.2:c.720+64T=	NP_001345462.1:n.720+64T=
NR_033233.2:n.899+64T=
NM_001358534.2:c.720+64T=	NP_001345463.1:n.720+64T=
NM_005943.6:c.981+64T=	NP_005934.2:n.981+64T=