Canonical Allele Identifier: CA2838628428

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098563del , CM000667.2:g.53098563del	GRCh38
NC_000005.9:g.52394393del , CM000667.1:g.52394393del	GRCh37
NC_000005.8:g.52430150del	NCBI36
NG_008435.2:g.16208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*41del MANE Select	ENSP00000380157.3:n.*41del
ENST00000450852.8:c.*528del MANE Plus Clinical	ENSP00000411022.3:n.*528del
ENST00000361377.8:c.*377del	ENSP00000355160.4:n.*377del
ENST00000396954.7:c.*41del	ENSP00000380157.3:n.*41del
ENST00000450852.7:c.*528del	ENSP00000411022.3:n.*528del
ENST00000502402.5:n.2355del
ENST00000508922.5:c.*448del	ENSP00000426274.1:n.*448del
ENST00000510818.6:c.*481del	ENSP00000424267.2:n.*481del
ENST00000582677.5:c.*249del	ENSP00000462870.1:n.*249del
ENST00000584946.5:c.*400del	ENSP00000464663.1:n.*400del
NM_004531.4:c.*41del	NP_004522.1:n.*41del
NM_176806.3:c.*528del	NP_789776.1:n.*528del
NM_004531.5:c.*41del MANE Select	NP_004522.1:n.*41del
NM_176806.4:c.*528del MANE Plus Clinical	NP_789776.1:n.*528del