Canonical Allele Identifier: CA1546395288

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098454_53098458delinsTCTTG , CM000667.2:g.53098454_53098458delinsTCTTG	GRCh38
NC_000005.9:g.52394284_52394288delinsTCTTG , CM000667.1:g.52394284_52394288delinsTCTTG	GRCh37
NC_000005.8:g.52430041_52430045delinsTCTTG	NCBI36
NG_008435.2:g.16311_16315delinsCAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*144_*148delinsCAAGA MANE Select	ENSP00000380157.3:n.*144_*148delinsCAAGA
ENST00000450852.8:c.*631_*635delinsCAAGA MANE Plus Clinical	ENSP00000411022.3:n.*631_*635delinsCAAGA
ENST00000361377.8:c.*480_*484delinsCAAGA	ENSP00000355160.4:n.*480_*484delinsCAAGA
ENST00000396954.7:c.*144_*148delinsCAAGA	ENSP00000380157.3:n.*144_*148delinsCAAGA
ENST00000450852.7:c.*631_*635delinsCAAGA	ENSP00000411022.3:n.*631_*635delinsCAAGA
ENST00000502402.5:n.2458_2462delinsCAAGA
ENST00000508922.5:c.*551_*555delinsCAAGA	ENSP00000426274.1:n.*551_*555delinsCAAGA
ENST00000510818.6:c.*584_*588delinsCAAGA	ENSP00000424267.2:n.*584_*588delinsCAAGA
ENST00000582677.5:c.*352_*356delinsCAAGA	ENSP00000462870.1:n.*352_*356delinsCAAGA
NM_004531.4:c.*144_*148delinsCAAGA	NP_004522.1:n.*144_*148delinsCAAGA
NM_176806.3:c.*631_*635delinsCAAGA	NP_789776.1:n.*631_*635delinsCAAGA
NM_004531.5:c.*144_*148delinsCAAGA MANE Select	NP_004522.1:n.*144_*148delinsCAAGA
NM_176806.4:c.*631_*635delinsCAAGA MANE Plus Clinical	NP_789776.1:n.*631_*635delinsCAAGA