Canonical Allele Identifier: CA1546395277

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098434T= , CM000667.2:g.53098434T=	GRCh38
NC_000005.9:g.52394264T= , CM000667.1:g.52394264T=	GRCh37
NC_000005.8:g.52430021T=	NCBI36
NG_008435.2:g.16335A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*168A= MANE Select	ENSP00000380157.3:n.*168A=
ENST00000450852.8:c.*655A= MANE Plus Clinical	ENSP00000411022.3:n.*655A=
ENST00000361377.8:c.*504A=	ENSP00000355160.4:n.*504A=
ENST00000396954.7:c.*168A=	ENSP00000380157.3:n.*168A=
ENST00000450852.7:c.*655A=	ENSP00000411022.3:n.*655A=
ENST00000502402.5:n.2482A=
ENST00000508922.5:c.*575A=	ENSP00000426274.1:n.*575A=
ENST00000510818.6:c.*608A=	ENSP00000424267.2:n.*608A=
ENST00000582677.5:c.*376A=	ENSP00000462870.1:n.*376A=
NM_004531.4:c.*168A=	NP_004522.1:n.*168A=
NM_176806.3:c.*655A=	NP_789776.1:n.*655A=
NM_004531.5:c.*168A= MANE Select	NP_004522.1:n.*168A=
NM_176806.4:c.*655A= MANE Plus Clinical	NP_789776.1:n.*655A=