Canonical Allele Identifier: CA1546395364

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098610T= , CM000667.2:g.53098610T=	GRCh38
NC_000005.9:g.52394440T= , CM000667.1:g.52394440T=	GRCh37
NC_000005.8:g.52430197T=	NCBI36
NG_008435.2:g.16159A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.559A= MANE Select	ENSP00000380157.3:p.Asn187=
ENST00000450852.8:c.*479A= MANE Plus Clinical	ENSP00000411022.3:n.*479A=
ENST00000361377.8:c.*328A=	ENSP00000355160.4:n.*328A=
ENST00000396954.7:c.559A=	ENSP00000380157.3:p.Asn187=
ENST00000450852.7:c.*479A=	ENSP00000411022.3:n.*479A=
ENST00000502402.5:n.2306A=
ENST00000508922.5:c.*399A=	ENSP00000426274.1:n.*399A=
ENST00000510818.6:c.*432A=	ENSP00000424267.2:n.*432A=
ENST00000582677.5:c.*200A=	ENSP00000462870.1:n.*200A=
ENST00000584946.5:c.*351A=	ENSP00000464663.1:n.*351A=
NM_004531.4:c.559A=	NP_004522.1:p.Asn187=
NM_176806.3:c.*479A=	NP_789776.1:n.*479A=
NM_004531.5:c.559A= MANE Select	NP_004522.1:p.Asn187=
NM_176806.4:c.*479A= MANE Plus Clinical	NP_789776.1:n.*479A=