Canonical Allele Identifier: CA1546395339

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098566C= , CM000667.2:g.53098566C=	GRCh38
NC_000005.9:g.52394396C= , CM000667.1:g.52394396C=	GRCh37
NC_000005.8:g.52430153C=	NCBI36
NG_008435.2:g.16203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*36G= MANE Select	ENSP00000380157.3:n.*36G=
ENST00000450852.8:c.*523G= MANE Plus Clinical	ENSP00000411022.3:n.*523G=
ENST00000361377.8:c.*372G=	ENSP00000355160.4:n.*372G=
ENST00000396954.7:c.*36G=	ENSP00000380157.3:n.*36G=
ENST00000450852.7:c.*523G=	ENSP00000411022.3:n.*523G=
ENST00000502402.5:n.2350G=
ENST00000508922.5:c.*443G=	ENSP00000426274.1:n.*443G=
ENST00000510818.6:c.*476G=	ENSP00000424267.2:n.*476G=
ENST00000582677.5:c.*244G=	ENSP00000462870.1:n.*244G=
ENST00000584946.5:c.*395G=	ENSP00000464663.1:n.*395G=
NM_004531.4:c.*36G=	NP_004522.1:n.*36G=
NM_176806.3:c.*523G=	NP_789776.1:n.*523G=
NM_004531.5:c.*36G= MANE Select	NP_004522.1:n.*36G=
NM_176806.4:c.*523G= MANE Plus Clinical	NP_789776.1:n.*523G=