Canonical Allele Identifier: CA1546399120
Gene: MOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53107052A= , CM000667.2:g.53107052A= GRCh38
NC_000005.9:g.52402882A= , CM000667.1:g.52402882A= GRCh37
NC_000005.8:g.52438639A= NCBI36
NG_008435.2:g.7717T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396954.8:c.98+25T= MANE Select ENSP00000380157.3:n.98+25T=
ENST00000450852.8:c.*18+25T= MANE Plus Clinical ENSP00000411022.3:n.*18+25T=
ENST00000361377.8:c.*18+25T= ENSP00000355160.4:n.*18+25T=
ENST00000396954.7:c.98+25T= ENSP00000380157.3:n.98+25T=
ENST00000450852.7:c.*18+25T= ENSP00000411022.3:n.*18+25T=
ENST00000502402.5:n.1021+25T=
ENST00000508922.5:c.*18+25T= ENSP00000426274.1:n.*18+25T=
ENST00000510818.6:c.*18+25T= ENSP00000424267.2:n.*18+25T=
ENST00000514553.2:n.283+25T=
ENST00000527216.5:c.*18+25T= ENSP00000435326.1:n.*18+25T=
ENST00000582677.5:c.*18+25T= ENSP00000462870.1:n.*18+25T=
ENST00000584946.5:c.*18+25T= ENSP00000464663.1:n.*18+25T=
NM_004531.4:c.98+25T= NP_004522.1:n.98+25T=
NM_176806.3:c.*18+25T= NP_789776.1:n.*18+25T=
NM_004531.5:c.98+25T= MANE Select NP_004522.1:n.98+25T=
NM_176806.4:c.*18+25T= MANE Plus Clinical NP_789776.1:n.*18+25T=