Canonical Allele Identifier: CA1546395359

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098602T= , CM000667.2:g.53098602T=	GRCh38
NC_000005.9:g.52394432T= , CM000667.1:g.52394432T=	GRCh37
NC_000005.8:g.52430189T=	NCBI36
NG_008435.2:g.16167A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.567A= MANE Select	ENSP00000380157.3:p.Ter189=
ENST00000450852.8:c.*487A= MANE Plus Clinical	ENSP00000411022.3:n.*487A=
ENST00000361377.8:c.*336A=	ENSP00000355160.4:n.*336A=
ENST00000396954.7:c.567A=	ENSP00000380157.3:p.Ter189=
ENST00000450852.7:c.*487A=	ENSP00000411022.3:n.*487A=
ENST00000502402.5:n.2314A=
ENST00000508922.5:c.*407A=	ENSP00000426274.1:n.*407A=
ENST00000510818.6:c.*440A=	ENSP00000424267.2:n.*440A=
ENST00000582677.5:c.*208A=	ENSP00000462870.1:n.*208A=
ENST00000584946.5:c.*359A=	ENSP00000464663.1:n.*359A=
NM_004531.4:c.567A=	NP_004522.1:p.Ter189=
NM_176806.3:c.*487A=	NP_789776.1:n.*487A=
NM_004531.5:c.567A= MANE Select	NP_004522.1:p.Ter189=
NM_176806.4:c.*487A= MANE Plus Clinical	NP_789776.1:n.*487A=