Canonical Allele Identifier: CA1546395348

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098581A= , CM000667.2:g.53098581A=	GRCh38
NC_000005.9:g.52394411A= , CM000667.1:g.52394411A=	GRCh37
NC_000005.8:g.52430168A=	NCBI36
NG_008435.2:g.16188T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*21T= MANE Select	ENSP00000380157.3:n.*21T=
ENST00000450852.8:c.*508T= MANE Plus Clinical	ENSP00000411022.3:n.*508T=
ENST00000361377.8:c.*357T=	ENSP00000355160.4:n.*357T=
ENST00000396954.7:c.*21T=	ENSP00000380157.3:n.*21T=
ENST00000450852.7:c.*508T=	ENSP00000411022.3:n.*508T=
ENST00000502402.5:n.2335T=
ENST00000508922.5:c.*428T=	ENSP00000426274.1:n.*428T=
ENST00000510818.6:c.*461T=	ENSP00000424267.2:n.*461T=
ENST00000582677.5:c.*229T=	ENSP00000462870.1:n.*229T=
ENST00000584946.5:c.*380T=	ENSP00000464663.1:n.*380T=
NM_004531.4:c.*21T=	NP_004522.1:n.*21T=
NM_176806.3:c.*508T=	NP_789776.1:n.*508T=
NM_004531.5:c.*21T= MANE Select	NP_004522.1:n.*21T=
NM_176806.4:c.*508T= MANE Plus Clinical	NP_789776.1:n.*508T=