Canonical Allele Identifier: CA1546399185

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107189G= , CM000667.2:g.53107189G=	GRCh38
NC_000005.9:g.52403019G= , CM000667.1:g.52403019G=	GRCh37
NC_000005.8:g.52438776G=	NCBI36
NG_008435.2:g.7580C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.-15C= MANE Select	ENSP00000380157.3:n.-15C=
ENST00000450852.8:c.173C= MANE Plus Clinical	ENSP00000411022.3:p.Ala58=
ENST00000361377.8:c.173C=	ENSP00000355160.4:p.Ala58=
ENST00000396954.7:c.-15C=	ENSP00000380157.3:n.-15C=
ENST00000450852.7:c.173C=	ENSP00000411022.3:p.Ala58=
ENST00000502402.5:n.909C=
ENST00000508922.5:c.173C=	ENSP00000426274.1:p.Ala58=
ENST00000510818.6:c.173C=	ENSP00000424267.2:p.Ala58=
ENST00000514553.2:n.171C=
ENST00000527216.5:c.158C=	ENSP00000435326.1:p.Ala53=
ENST00000582677.5:c.173C=	ENSP00000462870.1:p.Ala58=
ENST00000584946.5:c.173C=	ENSP00000464663.1:p.Ala58=
NM_004531.4:c.-15C=	NP_004522.1:n.-15C=
NM_176806.3:c.173C=	NP_789776.1:p.Ala58=
NM_004531.5:c.-15C= MANE Select	NP_004522.1:n.-15C=
NM_176806.4:c.173C= MANE Plus Clinical	NP_789776.1:p.Ala58=