Canonical Allele Identifier: CA1546395346

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098578T= , CM000667.2:g.53098578T=	GRCh38
NC_000005.9:g.52394408T= , CM000667.1:g.52394408T=	GRCh37
NC_000005.8:g.52430165T=	NCBI36
NG_008435.2:g.16191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*24A= MANE Select	ENSP00000380157.3:n.*24A=
ENST00000450852.8:c.*511A= MANE Plus Clinical	ENSP00000411022.3:n.*511A=
ENST00000361377.8:c.*360A=	ENSP00000355160.4:n.*360A=
ENST00000396954.7:c.*24A=	ENSP00000380157.3:n.*24A=
ENST00000450852.7:c.*511A=	ENSP00000411022.3:n.*511A=
ENST00000502402.5:n.2338A=
ENST00000508922.5:c.*431A=	ENSP00000426274.1:n.*431A=
ENST00000510818.6:c.*464A=	ENSP00000424267.2:n.*464A=
ENST00000582677.5:c.*232A=	ENSP00000462870.1:n.*232A=
ENST00000584946.5:c.*383A=	ENSP00000464663.1:n.*383A=
NM_004531.4:c.*24A=	NP_004522.1:n.*24A=
NM_176806.3:c.*511A=	NP_789776.1:n.*511A=
NM_004531.5:c.*24A= MANE Select	NP_004522.1:n.*24A=
NM_176806.4:c.*511A= MANE Plus Clinical	NP_789776.1:n.*511A=