Canonical Allele Identifier: CA1546395350

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098583G= , CM000667.2:g.53098583G=	GRCh38
NC_000005.9:g.52394413G= , CM000667.1:g.52394413G=	GRCh37
NC_000005.8:g.52430170G=	NCBI36
NG_008435.2:g.16186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*19C= MANE Select	ENSP00000380157.3:n.*19C=
ENST00000450852.8:c.*506C= MANE Plus Clinical	ENSP00000411022.3:n.*506C=
ENST00000361377.8:c.*355C=	ENSP00000355160.4:n.*355C=
ENST00000396954.7:c.*19C=	ENSP00000380157.3:n.*19C=
ENST00000450852.7:c.*506C=	ENSP00000411022.3:n.*506C=
ENST00000502402.5:n.2333C=
ENST00000508922.5:c.*426C=	ENSP00000426274.1:n.*426C=
ENST00000510818.6:c.*459C=	ENSP00000424267.2:n.*459C=
ENST00000582677.5:c.*227C=	ENSP00000462870.1:n.*227C=
ENST00000584946.5:c.*378C=	ENSP00000464663.1:n.*378C=
NM_004531.4:c.*19C=	NP_004522.1:n.*19C=
NM_176806.3:c.*506C=	NP_789776.1:n.*506C=
NM_004531.5:c.*19C= MANE Select	NP_004522.1:n.*19C=
NM_176806.4:c.*506C= MANE Plus Clinical	NP_789776.1:n.*506C=