Canonical Allele Identifier: CA1546395366

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098614T= , CM000667.2:g.53098614T=	GRCh38
NC_000005.9:g.52394444T= , CM000667.1:g.52394444T=	GRCh37
NC_000005.8:g.52430201T=	NCBI36
NG_008435.2:g.16155A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.555A= MANE Select	ENSP00000380157.3:p.Ala185=
ENST00000450852.8:c.*475A= MANE Plus Clinical	ENSP00000411022.3:n.*475A=
ENST00000361377.8:c.*324A=	ENSP00000355160.4:n.*324A=
ENST00000396954.7:c.555A=	ENSP00000380157.3:p.Ala185=
ENST00000450852.7:c.*475A=	ENSP00000411022.3:n.*475A=
ENST00000502402.5:n.2302A=
ENST00000508922.5:c.*395A=	ENSP00000426274.1:n.*395A=
ENST00000510818.6:c.*428A=	ENSP00000424267.2:n.*428A=
ENST00000582677.5:c.*196A=	ENSP00000462870.1:n.*196A=
ENST00000584946.5:c.*347A=	ENSP00000464663.1:n.*347A=
NM_004531.4:c.555A=	NP_004522.1:p.Ala185=
NM_176806.3:c.*475A=	NP_789776.1:n.*475A=
NM_004531.5:c.555A= MANE Select	NP_004522.1:p.Ala185=
NM_176806.4:c.*475A= MANE Plus Clinical	NP_789776.1:n.*475A=