Canonical Allele Identifier: CA1546399183

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107184G= , CM000667.2:g.53107184G=	GRCh38
NC_000005.9:g.52403014G= , CM000667.1:g.52403014G=	GRCh37
NC_000005.8:g.52438771G=	NCBI36
NG_008435.2:g.7585C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.-10C= MANE Select	ENSP00000380157.3:n.-10C=
ENST00000450852.8:c.178C= MANE Plus Clinical	ENSP00000411022.3:p.Arg60=
ENST00000361377.8:c.178C=	ENSP00000355160.4:p.Arg60=
ENST00000396954.7:c.-10C=	ENSP00000380157.3:n.-10C=
ENST00000450852.7:c.178C=	ENSP00000411022.3:p.Arg60=
ENST00000502402.5:n.914C=
ENST00000508922.5:c.178C=	ENSP00000426274.1:p.Arg60=
ENST00000510818.6:c.178C=	ENSP00000424267.2:p.Arg60=
ENST00000514553.2:n.176C=
ENST00000527216.5:c.163C=	ENSP00000435326.1:p.Arg55=
ENST00000582677.5:c.178C=	ENSP00000462870.1:p.Arg60=
ENST00000584946.5:c.178C=	ENSP00000464663.1:p.Arg60=
NM_004531.4:c.-10C=	NP_004522.1:n.-10C=
NM_176806.3:c.178C=	NP_789776.1:p.Arg60=
NM_004531.5:c.-10C= MANE Select	NP_004522.1:n.-10C=
NM_176806.4:c.178C= MANE Plus Clinical	NP_789776.1:p.Arg60=