Canonical Allele Identifier: CA1546395281

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098446C= , CM000667.2:g.53098446C=	GRCh38
NC_000005.9:g.52394276C= , CM000667.1:g.52394276C=	GRCh37
NC_000005.8:g.52430033C=	NCBI36
NG_008435.2:g.16323G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*156G= MANE Select	ENSP00000380157.3:n.*156G=
ENST00000450852.8:c.*643G= MANE Plus Clinical	ENSP00000411022.3:n.*643G=
ENST00000361377.8:c.*492G=	ENSP00000355160.4:n.*492G=
ENST00000396954.7:c.*156G=	ENSP00000380157.3:n.*156G=
ENST00000450852.7:c.*643G=	ENSP00000411022.3:n.*643G=
ENST00000502402.5:n.2470G=
ENST00000508922.5:c.*563G=	ENSP00000426274.1:n.*563G=
ENST00000510818.6:c.*596G=	ENSP00000424267.2:n.*596G=
ENST00000582677.5:c.*364G=	ENSP00000462870.1:n.*364G=
NM_004531.4:c.*156G=	NP_004522.1:n.*156G=
NM_176806.3:c.*643G=	NP_789776.1:n.*643G=
NM_004531.5:c.*156G= MANE Select	NP_004522.1:n.*156G=
NM_176806.4:c.*643G= MANE Plus Clinical	NP_789776.1:n.*643G=