Canonical Allele Identifier: CA1546395357

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098595T= , CM000667.2:g.53098595T=	GRCh38
NC_000005.9:g.52394425T= , CM000667.1:g.52394425T=	GRCh37
NC_000005.8:g.52430182T=	NCBI36
NG_008435.2:g.16174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*7A= MANE Select	ENSP00000380157.3:n.*7A=
ENST00000450852.8:c.*494A= MANE Plus Clinical	ENSP00000411022.3:n.*494A=
ENST00000361377.8:c.*343A=	ENSP00000355160.4:n.*343A=
ENST00000396954.7:c.*7A=	ENSP00000380157.3:n.*7A=
ENST00000450852.7:c.*494A=	ENSP00000411022.3:n.*494A=
ENST00000502402.5:n.2321A=
ENST00000508922.5:c.*414A=	ENSP00000426274.1:n.*414A=
ENST00000510818.6:c.*447A=	ENSP00000424267.2:n.*447A=
ENST00000582677.5:c.*215A=	ENSP00000462870.1:n.*215A=
ENST00000584946.5:c.*366A=	ENSP00000464663.1:n.*366A=
NM_004531.4:c.*7A=	NP_004522.1:n.*7A=
NM_176806.3:c.*494A=	NP_789776.1:n.*494A=
NM_004531.5:c.*7A= MANE Select	NP_004522.1:n.*7A=
NM_176806.4:c.*494A= MANE Plus Clinical	NP_789776.1:n.*494A=