Canonical Allele Identifier: CA1546395351

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098584C= , CM000667.2:g.53098584C=	GRCh38
NC_000005.9:g.52394414C= , CM000667.1:g.52394414C=	GRCh37
NC_000005.8:g.52430171C=	NCBI36
NG_008435.2:g.16185G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*18G= MANE Select	ENSP00000380157.3:n.*18G=
ENST00000450852.8:c.*505G= MANE Plus Clinical	ENSP00000411022.3:n.*505G=
ENST00000361377.8:c.*354G=	ENSP00000355160.4:n.*354G=
ENST00000396954.7:c.*18G=	ENSP00000380157.3:n.*18G=
ENST00000450852.7:c.*505G=	ENSP00000411022.3:n.*505G=
ENST00000502402.5:n.2332G=
ENST00000508922.5:c.*425G=	ENSP00000426274.1:n.*425G=
ENST00000510818.6:c.*458G=	ENSP00000424267.2:n.*458G=
ENST00000582677.5:c.*226G=	ENSP00000462870.1:n.*226G=
ENST00000584946.5:c.*377G=	ENSP00000464663.1:n.*377G=
NM_004531.4:c.*18G=	NP_004522.1:n.*18G=
NM_176806.3:c.*505G=	NP_789776.1:n.*505G=
NM_004531.5:c.*18G= MANE Select	NP_004522.1:n.*18G=
NM_176806.4:c.*505G= MANE Plus Clinical	NP_789776.1:n.*505G=