Canonical Allele Identifier: CA137652795
Community Standard Title: NM_001358530.2(MOCS1):c.421C>T (p.Gln141Ter)
Gene: MOCS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39916230G>A , CM000668.2:g.39916230G>A GRCh38
NC_000006.11:g.39883974G>A , CM000668.1:g.39883974G>A GRCh37
NC_000006.10:g.39991952G>A NCBI36
NG_009297.1:g.23281C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001358530.2:c.421C>T MANE Select NP_001345459.1:p.Gln141Ter
ENST00000340692.10:c.421C>T MANE Select ENSP00000344794.5:p.Gln141Ter
NM_001075098.3:c.421C>T NP_001068566.1:p.Gln141Ter
NM_001075098.4:c.421C>T NP_001068566.1:p.Gln141Ter
NM_001358529.1:c.421C>T NP_001345458.1:p.Gln141Ter
NM_001358529.2:c.421C>T NP_001345458.1:p.Gln141Ter
NM_001358530.1:c.421C>T NP_001345459.1:p.Gln141Ter
NM_001358531.1:c.160C>T NP_001345460.1:p.Gln54Ter
NM_001358531.2:c.160C>T NP_001345460.1:p.Gln54Ter
NM_001358533.1:c.160C>T NP_001345462.1:p.Gln54Ter
NM_001358533.2:c.160C>T NP_001345462.1:p.Gln54Ter
NM_001358534.1:c.160C>T NP_001345463.1:p.Gln54Ter
NM_001358534.2:c.160C>T NP_001345463.1:p.Gln54Ter
NM_005943.5:c.421C>T NP_005934.2:p.Gln141Ter
NM_005943.6:c.421C>T NP_005934.2:p.Gln141Ter
NR_033233.1:n.428C>T
NR_033233.2:n.339C>T
ENST00000340692.9:c.421C>T ENSP00000344794.5:p.Gln141Ter
ENST00000373181.8:c.160C>T ENSP00000362277.4:p.Gln54Ter
ENST00000373186.8:c.421C>T ENSP00000362282.4:p.Gln141Ter
ENST00000373188.6:c.421C>T ENSP00000362284.2:p.Gln141Ter
ENST00000373195.7:c.160C>T ENSP00000362291.3:p.Gln54Ter
ENST00000425303.6:c.421C>T ENSP00000416478.2:p.Gln141Ter
ENST00000432280.2:c.334C>T ENSP00000410809.2:p.Gln112Ter
ENST00000473742.1:n.301C>T
ENST00000645522.1:n.559C>T
XM_011514632.1:c.421C>T XP_011512934.1:p.Gln141Ter
XM_011514633.1:c.421C>T XP_011512935.1:p.Gln141Ter
XM_011514634.1:c.160C>T XP_011512936.1:p.Gln54Ter
XM_011514635.1:c.421C>T XP_011512937.1:p.Gln141Ter
XR_926225.1:n.466C>T