Canonical Allele Identifier: CA1622892960
Gene: MOCS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39912274C= , CM000668.2:g.39912274C= GRCh38
NC_000006.11:g.39880018C= , CM000668.1:g.39880018C= GRCh37
NC_000006.10:g.39987996C= NCBI36
NG_009297.1:g.27237G=

Transcript Alleles

HGVS Amino-acid Change
NM_001358530.2:c.971G= MANE Select NP_001345459.1:p.Gly324=
ENST00000340692.10:c.971G= MANE Select ENSP00000344794.5:p.Gly324=
NM_001075098.3:c.971G= NP_001068566.1:p.Gly324=
NM_001075098.4:c.971G= NP_001068566.1:p.Gly324=
NM_001358529.1:c.971G= NP_001345458.1:p.Gly324=
NM_001358529.2:c.971G= NP_001345458.1:p.Gly324=
NM_001358530.1:c.971G= NP_001345459.1:p.Gly324=
NM_001358531.1:c.710G= NP_001345460.1:p.Gly237=
NM_001358531.2:c.710G= NP_001345460.1:p.Gly237=
NM_001358533.1:c.710G= NP_001345462.1:p.Gly237=
NM_001358533.2:c.710G= NP_001345462.1:p.Gly237=
NM_001358534.1:c.710G= NP_001345463.1:p.Gly237=
NM_001358534.2:c.710G= NP_001345463.1:p.Gly237=
NM_005943.5:c.971G= NP_005934.2:p.Gly324=
NM_005943.6:c.971G= NP_005934.2:p.Gly324=
NR_033233.1:n.978G=
NR_033233.2:n.889G=
ENST00000340692.9:c.971G= ENSP00000344794.5:p.Gly324=
ENST00000373181.8:c.710G= ENSP00000362277.4:p.Gly237=
ENST00000373186.8:c.971G= ENSP00000362282.4:p.Gly324=
ENST00000373188.6:c.971G= ENSP00000362284.2:p.Gly324=
ENST00000373195.7:c.710G= ENSP00000362291.3:p.Gly237=
ENST00000425303.6:c.971G= ENSP00000416478.2:p.Gly324=
ENST00000432280.2:c.884G= ENSP00000410809.2:p.Gly295=
ENST00000645522.1:n.1109G=
XM_011514632.1:c.971G= XP_011512934.1:p.Gly324=
XM_011514633.1:c.971G= XP_011512935.1:p.Gly324=
XM_011514634.1:c.710G= XP_011512936.1:p.Gly237=
XM_011514635.1:c.971G= XP_011512937.1:p.Gly324=
XR_926225.1:n.1016G=