Canonical Allele Identifier: CA1546395398
Gene: MOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53098682C= , CM000667.2:g.53098682C= GRCh38
NC_000005.9:g.52394512C= , CM000667.1:g.52394512C= GRCh37
NC_000005.8:g.52430269C= NCBI36
NG_008435.2:g.16087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396954.8:c.502-15G= MANE Select ENSP00000380157.3:n.502-15G=
ENST00000450852.8:c.*422-15G= MANE Plus Clinical ENSP00000411022.3:n.*422-15G=
ENST00000361377.8:c.*271-15G= ENSP00000355160.4:n.*271-15G=
ENST00000396954.7:c.502-15G= ENSP00000380157.3:n.502-15G=
ENST00000450852.7:c.*422-15G= ENSP00000411022.3:n.*422-15G=
ENST00000502402.5:n.2249-15G=
ENST00000508922.5:c.*327G= ENSP00000426274.1:n.*327G=
ENST00000510818.6:c.*375-15G= ENSP00000424267.2:n.*375-15G=
ENST00000582677.5:c.*143-15G= ENSP00000462870.1:n.*143-15G=
ENST00000584946.5:c.*294-15G= ENSP00000464663.1:n.*294-15G=
NM_004531.4:c.502-15G= NP_004522.1:n.502-15G=
NM_176806.3:c.*422-15G= NP_789776.1:n.*422-15G=
NM_004531.5:c.502-15G= MANE Select NP_004522.1:n.502-15G=
NM_176806.4:c.*422-15G= MANE Plus Clinical NP_789776.1:n.*422-15G=