Canonical Allele Identifier: CA1546395341

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098569A= , CM000667.2:g.53098569A=	GRCh38
NC_000005.9:g.52394399A= , CM000667.1:g.52394399A=	GRCh37
NC_000005.8:g.52430156A=	NCBI36
NG_008435.2:g.16200T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*33T= MANE Select	ENSP00000380157.3:n.*33T=
ENST00000450852.8:c.*520T= MANE Plus Clinical	ENSP00000411022.3:n.*520T=
ENST00000361377.8:c.*369T=	ENSP00000355160.4:n.*369T=
ENST00000396954.7:c.*33T=	ENSP00000380157.3:n.*33T=
ENST00000450852.7:c.*520T=	ENSP00000411022.3:n.*520T=
ENST00000502402.5:n.2347T=
ENST00000508922.5:c.*440T=	ENSP00000426274.1:n.*440T=
ENST00000510818.6:c.*473T=	ENSP00000424267.2:n.*473T=
ENST00000582677.5:c.*241T=	ENSP00000462870.1:n.*241T=
ENST00000584946.5:c.*392T=	ENSP00000464663.1:n.*392T=
NM_004531.4:c.*33T=	NP_004522.1:n.*33T=
NM_176806.3:c.*520T=	NP_789776.1:n.*520T=
NM_004531.5:c.*33T= MANE Select	NP_004522.1:n.*33T=
NM_176806.4:c.*520T= MANE Plus Clinical	NP_789776.1:n.*520T=