Canonical Allele Identifier: CA1546395355

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098593C= , CM000667.2:g.53098593C=	GRCh38
NC_000005.9:g.52394423C= , CM000667.1:g.52394423C=	GRCh37
NC_000005.8:g.52430180C=	NCBI36
NG_008435.2:g.16176G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*9G= MANE Select	ENSP00000380157.3:n.*9G=
ENST00000450852.8:c.*496G= MANE Plus Clinical	ENSP00000411022.3:n.*496G=
ENST00000361377.8:c.*345G=	ENSP00000355160.4:n.*345G=
ENST00000396954.7:c.*9G=	ENSP00000380157.3:n.*9G=
ENST00000450852.7:c.*496G=	ENSP00000411022.3:n.*496G=
ENST00000502402.5:n.2323G=
ENST00000508922.5:c.*416G=	ENSP00000426274.1:n.*416G=
ENST00000510818.6:c.*449G=	ENSP00000424267.2:n.*449G=
ENST00000582677.5:c.*217G=	ENSP00000462870.1:n.*217G=
ENST00000584946.5:c.*368G=	ENSP00000464663.1:n.*368G=
NM_004531.4:c.*9G=	NP_004522.1:n.*9G=
NM_176806.3:c.*496G=	NP_789776.1:n.*496G=
NM_004531.5:c.*9G= MANE Select	NP_004522.1:n.*9G=
NM_176806.4:c.*496G= MANE Plus Clinical	NP_789776.1:n.*496G=