Canonical Allele Identifier: CA1546395349

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098582T= , CM000667.2:g.53098582T=	GRCh38
NC_000005.9:g.52394412T= , CM000667.1:g.52394412T=	GRCh37
NC_000005.8:g.52430169T=	NCBI36
NG_008435.2:g.16187A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*20A= MANE Select	ENSP00000380157.3:n.*20A=
ENST00000450852.8:c.*507A= MANE Plus Clinical	ENSP00000411022.3:n.*507A=
ENST00000361377.8:c.*356A=	ENSP00000355160.4:n.*356A=
ENST00000396954.7:c.*20A=	ENSP00000380157.3:n.*20A=
ENST00000450852.7:c.*507A=	ENSP00000411022.3:n.*507A=
ENST00000502402.5:n.2334A=
ENST00000508922.5:c.*427A=	ENSP00000426274.1:n.*427A=
ENST00000510818.6:c.*460A=	ENSP00000424267.2:n.*460A=
ENST00000582677.5:c.*228A=	ENSP00000462870.1:n.*228A=
ENST00000584946.5:c.*379A=	ENSP00000464663.1:n.*379A=
NM_004531.4:c.*20A=	NP_004522.1:n.*20A=
NM_176806.3:c.*507A=	NP_789776.1:n.*507A=
NM_004531.5:c.*20A= MANE Select	NP_004522.1:n.*20A=
NM_176806.4:c.*507A= MANE Plus Clinical	NP_789776.1:n.*507A=