Canonical Allele Identifier: CA1546395360

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098603T= , CM000667.2:g.53098603T=	GRCh38
NC_000005.9:g.52394433T= , CM000667.1:g.52394433T=	GRCh37
NC_000005.8:g.52430190T=	NCBI36
NG_008435.2:g.16166A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.566A= MANE Select	ENSP00000380157.3:p.Ter189=
ENST00000450852.8:c.*486A= MANE Plus Clinical	ENSP00000411022.3:n.*486A=
ENST00000361377.8:c.*335A=	ENSP00000355160.4:n.*335A=
ENST00000396954.7:c.566A=	ENSP00000380157.3:p.Ter189=
ENST00000450852.7:c.*486A=	ENSP00000411022.3:n.*486A=
ENST00000502402.5:n.2313A=
ENST00000508922.5:c.*406A=	ENSP00000426274.1:n.*406A=
ENST00000510818.6:c.*439A=	ENSP00000424267.2:n.*439A=
ENST00000582677.5:c.*207A=	ENSP00000462870.1:n.*207A=
ENST00000584946.5:c.*358A=	ENSP00000464663.1:n.*358A=
NM_004531.4:c.566A=	NP_004522.1:p.Ter189=
NM_176806.3:c.*486A=	NP_789776.1:n.*486A=
NM_004531.5:c.566A= MANE Select	NP_004522.1:p.Ter189=
NM_176806.4:c.*486A= MANE Plus Clinical	NP_789776.1:n.*486A=