Canonical Allele Identifier: CA1546395342

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098570G= , CM000667.2:g.53098570G=	GRCh38
NC_000005.9:g.52394400G= , CM000667.1:g.52394400G=	GRCh37
NC_000005.8:g.52430157G=	NCBI36
NG_008435.2:g.16199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*32C= MANE Select	ENSP00000380157.3:n.*32C=
ENST00000450852.8:c.*519C= MANE Plus Clinical	ENSP00000411022.3:n.*519C=
ENST00000361377.8:c.*368C=	ENSP00000355160.4:n.*368C=
ENST00000396954.7:c.*32C=	ENSP00000380157.3:n.*32C=
ENST00000450852.7:c.*519C=	ENSP00000411022.3:n.*519C=
ENST00000502402.5:n.2346C=
ENST00000508922.5:c.*439C=	ENSP00000426274.1:n.*439C=
ENST00000510818.6:c.*472C=	ENSP00000424267.2:n.*472C=
ENST00000582677.5:c.*240C=	ENSP00000462870.1:n.*240C=
ENST00000584946.5:c.*391C=	ENSP00000464663.1:n.*391C=
NM_004531.4:c.*32C=	NP_004522.1:n.*32C=
NM_176806.3:c.*519C=	NP_789776.1:n.*519C=
NM_004531.5:c.*32C= MANE Select	NP_004522.1:n.*32C=
NM_176806.4:c.*519C= MANE Plus Clinical	NP_789776.1:n.*519C=