Canonical Allele Identifier: CA1546395352

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098587T= , CM000667.2:g.53098587T=	GRCh38
NC_000005.9:g.52394417T= , CM000667.1:g.52394417T=	GRCh37
NC_000005.8:g.52430174T=	NCBI36
NG_008435.2:g.16182A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*15A= MANE Select	ENSP00000380157.3:n.*15A=
ENST00000450852.8:c.*502A= MANE Plus Clinical	ENSP00000411022.3:n.*502A=
ENST00000361377.8:c.*351A=	ENSP00000355160.4:n.*351A=
ENST00000396954.7:c.*15A=	ENSP00000380157.3:n.*15A=
ENST00000450852.7:c.*502A=	ENSP00000411022.3:n.*502A=
ENST00000502402.5:n.2329A=
ENST00000508922.5:c.*422A=	ENSP00000426274.1:n.*422A=
ENST00000510818.6:c.*455A=	ENSP00000424267.2:n.*455A=
ENST00000582677.5:c.*223A=	ENSP00000462870.1:n.*223A=
ENST00000584946.5:c.*374A=	ENSP00000464663.1:n.*374A=
NM_004531.4:c.*15A=	NP_004522.1:n.*15A=
NM_176806.3:c.*502A=	NP_789776.1:n.*502A=
NM_004531.5:c.*15A= MANE Select	NP_004522.1:n.*15A=
NM_176806.4:c.*502A= MANE Plus Clinical	NP_789776.1:n.*502A=