Canonical Allele Identifier: CA1546395328

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098549_53098552delinsCAAT , CM000667.2:g.53098549_53098552delinsCAAT	GRCh38
NC_000005.9:g.52394379_52394382delinsCAAT , CM000667.1:g.52394379_52394382delinsCAAT	GRCh37
NC_000005.8:g.52430136_52430139delinsCAAT	NCBI36
NG_008435.2:g.16217_16220delinsATTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*50_*53delinsATTG MANE Select	ENSP00000380157.3:n.*50_*53delinsATTG
ENST00000450852.8:c.*537_*540delinsATTG MANE Plus Clinical	ENSP00000411022.3:n.*537_*540delinsATTG
ENST00000361377.8:c.*386_*389delinsATTG	ENSP00000355160.4:n.*386_*389delinsATTG
ENST00000396954.7:c.*50_*53delinsATTG	ENSP00000380157.3:n.*50_*53delinsATTG
ENST00000450852.7:c.*537_*540delinsATTG	ENSP00000411022.3:n.*537_*540delinsATTG
ENST00000502402.5:n.2364_2367delinsATTG
ENST00000508922.5:c.*457_*460delinsATTG	ENSP00000426274.1:n.*457_*460delinsATTG
ENST00000510818.6:c.*490_*493delinsATTG	ENSP00000424267.2:n.*490_*493delinsATTG
ENST00000582677.5:c.*258_*261delinsATTG	ENSP00000462870.1:n.*258_*261delinsATTG
ENST00000584946.5:c.*409_*412delinsATTG	ENSP00000464663.1:n.*409_*412delinsATTG
NM_004531.4:c.*50_*53delinsATTG	NP_004522.1:n.*50_*53delinsATTG
NM_176806.3:c.*537_*540delinsATTG	NP_789776.1:n.*537_*540delinsATTG
NM_004531.5:c.*50_*53delinsATTG MANE Select	NP_004522.1:n.*50_*53delinsATTG
NM_176806.4:c.*537_*540delinsATTG MANE Plus Clinical	NP_789776.1:n.*537_*540delinsATTG