Canonical Allele Identifier: CA1546399184

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107186A= , CM000667.2:g.53107186A=	GRCh38
NC_000005.9:g.52403016A= , CM000667.1:g.52403016A=	GRCh37
NC_000005.8:g.52438773A=	NCBI36
NG_008435.2:g.7583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.-12T= MANE Select	ENSP00000380157.3:n.-12T=
ENST00000450852.8:c.176T= MANE Plus Clinical	ENSP00000411022.3:p.Val59=
ENST00000361377.8:c.176T=	ENSP00000355160.4:p.Val59=
ENST00000396954.7:c.-12T=	ENSP00000380157.3:n.-12T=
ENST00000450852.7:c.176T=	ENSP00000411022.3:p.Val59=
ENST00000502402.5:n.912T=
ENST00000508922.5:c.176T=	ENSP00000426274.1:p.Val59=
ENST00000510818.6:c.176T=	ENSP00000424267.2:p.Val59=
ENST00000514553.2:n.174T=
ENST00000527216.5:c.161T=	ENSP00000435326.1:p.Val54=
ENST00000582677.5:c.176T=	ENSP00000462870.1:p.Val59=
ENST00000584946.5:c.176T=	ENSP00000464663.1:p.Val59=
NM_004531.4:c.-12T=	NP_004522.1:n.-12T=
NM_176806.3:c.176T=	NP_789776.1:p.Val59=
NM_004531.5:c.-12T= MANE Select	NP_004522.1:n.-12T=
NM_176806.4:c.176T= MANE Plus Clinical	NP_789776.1:p.Val59=