Canonical Allele Identifier: CA364045210
Community Standard Title: NM_001358530.2(MOCS1):c.124-1G>T
Gene: MOCS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39927456C>A , CM000668.2:g.39927456C>A GRCh38
NC_000006.11:g.39895195C>A , CM000668.1:g.39895195C>A GRCh37
NC_000006.10:g.40003173C>A NCBI36
NG_009297.1:g.12060G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001358530.2:c.124-1G>T MANE Select NP_001345459.1:n.124-1G>T
ENST00000340692.10:c.124-1G>T MANE Select ENSP00000344794.5:n.124-1G>T
NM_001075098.3:c.124-1G>T NP_001068566.1:n.124-1G>T
NM_001075098.4:c.124-1G>T NP_001068566.1:n.124-1G>T
NM_001358529.1:c.124-1G>T NP_001345458.1:n.124-1G>T
NM_001358529.2:c.124-1G>T NP_001345458.1:n.124-1G>T
NM_001358530.1:c.124-1G>T NP_001345459.1:n.124-1G>T
NM_001358531.1:c.-11-1611G>T NP_001345460.1:n.-11-1611G>T
NM_001358531.2:c.-11-1611G>T NP_001345460.1:n.-11-1611G>T
NM_001358533.1:c.-11-1611G>T NP_001345462.1:n.-11-1611G>T
NM_001358533.2:c.-11-1611G>T NP_001345462.1:n.-11-1611G>T
NM_001358534.1:c.-138-1G>T NP_001345463.1:n.-138-1G>T
NM_001358534.2:c.-138-1G>T NP_001345463.1:n.-138-1G>T
NM_005943.5:c.123G>T NP_005934.2:p.Gln41His
NM_005943.6:c.123G>T NP_005934.2:p.Gln41His
NR_033233.1:n.258-1611G>T
NR_033233.2:n.169-1611G>T
ENST00000340692.9:c.124-1G>T ENSP00000344794.5:n.124-1G>T
ENST00000373181.8:c.-138-1G>T ENSP00000362277.4:n.-138-1G>T
ENST00000373186.8:c.123G>T ENSP00000362282.4:p.Gln41His
ENST00000373188.6:c.124-1G>T ENSP00000362284.2:n.124-1G>T
ENST00000373195.7:c.-11-1611G>T ENSP00000362291.3:n.-11-1611G>T
ENST00000425303.6:c.123G>T ENSP00000416478.2:p.Gln41His
ENST00000432280.2:c.37-1G>T ENSP00000410809.2:n.37-1G>T
ENST00000473742.1:n.131-1611G>T
ENST00000487924.1:c.124-1G>T ENSP00000418315.1:n.124-1G>T
ENST00000645522.1:n.261G>T
XM_011514632.1:c.124-1G>T XP_011512934.1:n.124-1G>T
XM_011514633.1:c.124-1G>T XP_011512935.1:n.124-1G>T
XM_011514634.1:c.-11-1611G>T XP_011512936.1:n.-11-1611G>T
XM_011514635.1:c.124-1G>T XP_011512937.1:n.124-1G>T
XR_926225.1:n.169-1G>T