Canonical Allele Identifier: CA1546399138

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107095C= , CM000667.2:g.53107095C=	GRCh38
NC_000005.9:g.52402925C= , CM000667.1:g.52402925C=	GRCh37
NC_000005.8:g.52438682C=	NCBI36
NG_008435.2:g.7674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.80G= MANE Select	ENSP00000380157.3:p.Ser27=
ENST00000450852.8:c.267G= MANE Plus Clinical	ENSP00000411022.3:p.Ter89=
ENST00000361377.8:c.267G=	ENSP00000355160.4:p.Ter89=
ENST00000396954.7:c.80G=	ENSP00000380157.3:p.Ser27=
ENST00000450852.7:c.267G=	ENSP00000411022.3:p.Ter89=
ENST00000502402.5:n.1003G=
ENST00000508922.5:c.267G=	ENSP00000426274.1:p.Ter89=
ENST00000510818.6:c.267G=	ENSP00000424267.2:p.Ter89=
ENST00000514553.2:n.265G=
ENST00000527216.5:c.252G=	ENSP00000435326.1:p.Ter84=
ENST00000582677.5:c.267G=	ENSP00000462870.1:p.Ter89=
ENST00000584946.5:c.267G=	ENSP00000464663.1:p.Ter89=
NM_004531.4:c.80G=	NP_004522.1:p.Ser27=
NM_176806.3:c.267G=	NP_789776.1:p.Ter89=
NM_004531.5:c.80G= MANE Select	NP_004522.1:p.Ser27=
NM_176806.4:c.267G= MANE Plus Clinical	NP_789776.1:p.Ter89=