Canonical Allele Identifier: CA3796256
Gene: MOCS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 356663
dbSNP Id: rs143573353
gnomAD v2: 6-39883875-C-T
gnomAD v3: 6-39916131-C-T
gnomAD v4: 6-39916131-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39916131C>T , CM000668.2:g.39916131C>T GRCh38
NC_000006.11:g.39883875C>T , CM000668.1:g.39883875C>T GRCh37
NC_000006.10:g.39991853C>T NCBI36
NG_009297.1:g.23380G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340692.10:c.520G>A MANE Select ENSP00000344794.5:p.Ala174Thr
ENST00000645522.1:n.658G>A
ENST00000340692.9:c.520G>A ENSP00000344794.5:p.Ala174Thr
ENST00000373181.8:c.259G>A ENSP00000362277.4:p.Ala87Thr
ENST00000373186.8:c.520G>A ENSP00000362282.4:p.Ala174Thr
ENST00000373188.6:c.520G>A ENSP00000362284.2:p.Ala174Thr
ENST00000373195.7:c.259G>A ENSP00000362291.3:p.Ala87Thr
ENST00000425303.6:c.520G>A ENSP00000416478.2:p.Ala174Thr
ENST00000432280.2:c.433G>A ENSP00000410809.2:p.Ala145Thr
ENST00000473742.1:n.400G>A
NM_001075098.3:c.520G>A NP_001068566.1:p.Ala174Thr
NM_005943.5:c.520G>A NP_005934.2:p.Ala174Thr
NR_033233.1:n.527G>A
XM_011514632.1:c.520G>A XP_011512934.1:p.Ala174Thr
XM_011514633.1:c.520G>A XP_011512935.1:p.Ala174Thr
XM_011514634.1:c.259G>A XP_011512936.1:p.Ala87Thr
XM_011514635.1:c.520G>A XP_011512937.1:p.Ala174Thr
XR_926225.1:n.565G>A
NM_001358529.1:c.520G>A NP_001345458.1:p.Ala174Thr
NM_001358530.1:c.520G>A NP_001345459.1:p.Ala174Thr
NM_001358531.1:c.259G>A NP_001345460.1:p.Ala87Thr
NM_001358533.1:c.259G>A NP_001345462.1:p.Ala87Thr
NM_001358534.1:c.259G>A NP_001345463.1:p.Ala87Thr
NM_001358530.2:c.520G>A MANE Select NP_001345459.1:p.Ala174Thr
NM_001075098.4:c.520G>A NP_001068566.1:p.Ala174Thr
NM_001358529.2:c.520G>A NP_001345458.1:p.Ala174Thr
NM_001358531.2:c.259G>A NP_001345460.1:p.Ala87Thr
NM_001358533.2:c.259G>A NP_001345462.1:p.Ala87Thr
NR_033233.2:n.438G>A
NM_001358534.2:c.259G>A NP_001345463.1:p.Ala87Thr
NM_005943.6:c.520G>A NP_005934.2:p.Ala174Thr