Canonical Allele Identifier: CA1546395347

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098580C= , CM000667.2:g.53098580C=	GRCh38
NC_000005.9:g.52394410C= , CM000667.1:g.52394410C=	GRCh37
NC_000005.8:g.52430167C=	NCBI36
NG_008435.2:g.16189G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*22G= MANE Select	ENSP00000380157.3:n.*22G=
ENST00000450852.8:c.*509G= MANE Plus Clinical	ENSP00000411022.3:n.*509G=
ENST00000361377.8:c.*358G=	ENSP00000355160.4:n.*358G=
ENST00000396954.7:c.*22G=	ENSP00000380157.3:n.*22G=
ENST00000450852.7:c.*509G=	ENSP00000411022.3:n.*509G=
ENST00000502402.5:n.2336G=
ENST00000508922.5:c.*429G=	ENSP00000426274.1:n.*429G=
ENST00000510818.6:c.*462G=	ENSP00000424267.2:n.*462G=
ENST00000582677.5:c.*230G=	ENSP00000462870.1:n.*230G=
ENST00000584946.5:c.*381G=	ENSP00000464663.1:n.*381G=
NM_004531.4:c.*22G=	NP_004522.1:n.*22G=
NM_176806.3:c.*509G=	NP_789776.1:n.*509G=
NM_004531.5:c.*22G= MANE Select	NP_004522.1:n.*22G=
NM_176806.4:c.*509G= MANE Plus Clinical	NP_789776.1:n.*509G=