Canonical Allele Identifier: CA1546395333

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098555_53098556delinsTA , CM000667.2:g.53098555_53098556delinsTA	GRCh38
NC_000005.9:g.52394385_52394386delinsTA , CM000667.1:g.52394385_52394386delinsTA	GRCh37
NC_000005.8:g.52430142_52430143delinsTA	NCBI36
NG_008435.2:g.16213_16214delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*46_*47delinsTA MANE Select	ENSP00000380157.3:n.*46_*47delinsTA
ENST00000450852.8:c.*533_*534delinsTA MANE Plus Clinical	ENSP00000411022.3:n.*533_*534delinsTA
ENST00000361377.8:c.*382_*383delinsTA	ENSP00000355160.4:n.*382_*383delinsTA
ENST00000396954.7:c.*46_*47delinsTA	ENSP00000380157.3:n.*46_*47delinsTA
ENST00000450852.7:c.*533_*534delinsTA	ENSP00000411022.3:n.*533_*534delinsTA
ENST00000502402.5:n.2360_2361delinsTA
ENST00000508922.5:c.*453_*454delinsTA	ENSP00000426274.1:n.*453_*454delinsTA
ENST00000510818.6:c.*486_*487delinsTA	ENSP00000424267.2:n.*486_*487delinsTA
ENST00000582677.5:c.*254_*255delinsTA	ENSP00000462870.1:n.*254_*255delinsTA
ENST00000584946.5:c.*405_*406delinsTA	ENSP00000464663.1:n.*405_*406delinsTA
NM_004531.4:c.*46_*47delinsTA	NP_004522.1:n.*46_*47delinsTA
NM_176806.3:c.*533_*534delinsTA	NP_789776.1:n.*533_*534delinsTA
NM_004531.5:c.*46_*47delinsTA MANE Select	NP_004522.1:n.*46_*47delinsTA
NM_176806.4:c.*533_*534delinsTA MANE Plus Clinical	NP_789776.1:n.*533_*534delinsTA