Canonical Allele Identifier: CA1546395353

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098588A= , CM000667.2:g.53098588A=	GRCh38
NC_000005.9:g.52394418A= , CM000667.1:g.52394418A=	GRCh37
NC_000005.8:g.52430175A=	NCBI36
NG_008435.2:g.16181T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*14T= MANE Select	ENSP00000380157.3:n.*14T=
ENST00000450852.8:c.*501T= MANE Plus Clinical	ENSP00000411022.3:n.*501T=
ENST00000361377.8:c.*350T=	ENSP00000355160.4:n.*350T=
ENST00000396954.7:c.*14T=	ENSP00000380157.3:n.*14T=
ENST00000450852.7:c.*501T=	ENSP00000411022.3:n.*501T=
ENST00000502402.5:n.2328T=
ENST00000508922.5:c.*421T=	ENSP00000426274.1:n.*421T=
ENST00000510818.6:c.*454T=	ENSP00000424267.2:n.*454T=
ENST00000582677.5:c.*222T=	ENSP00000462870.1:n.*222T=
ENST00000584946.5:c.*373T=	ENSP00000464663.1:n.*373T=
NM_004531.4:c.*14T=	NP_004522.1:n.*14T=
NM_176806.3:c.*501T=	NP_789776.1:n.*501T=
NM_004531.5:c.*14T= MANE Select	NP_004522.1:n.*14T=
NM_176806.4:c.*501T= MANE Plus Clinical	NP_789776.1:n.*501T=