Canonical Allele Identifier: CA2678649356

Gene: MOCS1

Linked Data

• gnomAD v4: 6-39912193-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39912193G>T , CM000668.2:g.39912193G>T	GRCh38
NC_000006.11:g.39879937G>T , CM000668.1:g.39879937G>T	GRCh37
NC_000006.10:g.39987915G>T	NCBI36
NG_009297.1:g.27318C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340692.10:c.981+71C>A MANE Select	ENSP00000344794.5:n.981+71C>A
ENST00000645522.1:n.1119+71C>A
ENST00000340692.9:c.981+71C>A	ENSP00000344794.5:n.981+71C>A
ENST00000373181.8:c.720+71C>A	ENSP00000362277.4:n.720+71C>A
ENST00000373186.8:c.981+71C>A	ENSP00000362282.4:n.981+71C>A
ENST00000373188.6:c.981+71C>A	ENSP00000362284.2:n.981+71C>A
ENST00000373195.7:c.720+71C>A	ENSP00000362291.3:n.720+71C>A
ENST00000425303.6:c.981+71C>A	ENSP00000416478.2:n.981+71C>A
ENST00000432280.2:c.894+71C>A	ENSP00000410809.2:n.894+71C>A
NM_001075098.3:c.981+71C>A	NP_001068566.1:n.981+71C>A
NM_005943.5:c.981+71C>A	NP_005934.2:n.981+71C>A
NR_033233.1:n.988+71C>A
XM_011514632.1:c.981+71C>A	XP_011512934.1:n.981+71C>A
XM_011514633.1:c.981+71C>A	XP_011512935.1:n.981+71C>A
XM_011514634.1:c.720+71C>A	XP_011512936.1:n.720+71C>A
XM_011514635.1:c.981+71C>A	XP_011512937.1:n.981+71C>A
XR_926225.1:n.1026+71C>A
NM_001358529.1:c.981+71C>A	NP_001345458.1:n.981+71C>A
NM_001358530.1:c.981+71C>A	NP_001345459.1:n.981+71C>A
NM_001358531.1:c.720+71C>A	NP_001345460.1:n.720+71C>A
NM_001358533.1:c.720+71C>A	NP_001345462.1:n.720+71C>A
NM_001358534.1:c.720+71C>A	NP_001345463.1:n.720+71C>A
NM_001358530.2:c.981+71C>A MANE Select	NP_001345459.1:n.981+71C>A
NM_001075098.4:c.981+71C>A	NP_001068566.1:n.981+71C>A
NM_001358529.2:c.981+71C>A	NP_001345458.1:n.981+71C>A
NM_001358531.2:c.720+71C>A	NP_001345460.1:n.720+71C>A
NM_001358533.2:c.720+71C>A	NP_001345462.1:n.720+71C>A
NR_033233.2:n.899+71C>A
NM_001358534.2:c.720+71C>A	NP_001345463.1:n.720+71C>A
NM_005943.6:c.981+71C>A	NP_005934.2:n.981+71C>A