Canonical Allele Identifier: CA1546399141

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107100C= , CM000667.2:g.53107100C=	GRCh38
NC_000005.9:g.52402930C= , CM000667.1:g.52402930C=	GRCh37
NC_000005.8:g.52438687C=	NCBI36
NG_008435.2:g.7669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.75G= MANE Select	ENSP00000380157.3:p.Glu25=
ENST00000450852.8:c.262G= MANE Plus Clinical	ENSP00000411022.3:p.Gly88=
ENST00000361377.8:c.262G=	ENSP00000355160.4:p.Gly88=
ENST00000396954.7:c.75G=	ENSP00000380157.3:p.Glu25=
ENST00000450852.7:c.262G=	ENSP00000411022.3:p.Gly88=
ENST00000502402.5:n.998G=
ENST00000508922.5:c.262G=	ENSP00000426274.1:p.Gly88=
ENST00000510818.6:c.262G=	ENSP00000424267.2:p.Gly88=
ENST00000514553.2:n.260G=
ENST00000527216.5:c.247G=	ENSP00000435326.1:p.Gly83=
ENST00000582677.5:c.262G=	ENSP00000462870.1:p.Gly88=
ENST00000584946.5:c.262G=	ENSP00000464663.1:p.Gly88=
NM_004531.4:c.75G=	NP_004522.1:p.Glu25=
NM_176806.3:c.262G=	NP_789776.1:p.Gly88=
NM_004531.5:c.75G= MANE Select	NP_004522.1:p.Glu25=
NM_176806.4:c.262G= MANE Plus Clinical	NP_789776.1:p.Gly88=