Canonical Allele Identifier: CA2673822462

Gene: MOCS2

Linked Data

• gnomAD v4: 5-53098437-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098439dup , CM000667.2:g.53098439dup	GRCh38
NC_000005.9:g.52394269dup , CM000667.1:g.52394269dup	GRCh37
NC_000005.8:g.52430026dup	NCBI36
NG_008435.2:g.16331dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*164dup MANE Select	ENSP00000380157.3:n.*164dup
ENST00000450852.8:c.*651dup MANE Plus Clinical	ENSP00000411022.3:n.*651dup
ENST00000361377.8:c.*500dup	ENSP00000355160.4:n.*500dup
ENST00000396954.7:c.*164dup	ENSP00000380157.3:n.*164dup
ENST00000450852.7:c.*651dup	ENSP00000411022.3:n.*651dup
ENST00000502402.5:n.2478dup
ENST00000508922.5:c.*571dup	ENSP00000426274.1:n.*571dup
ENST00000510818.6:c.*604dup	ENSP00000424267.2:n.*604dup
ENST00000582677.5:c.*372dup	ENSP00000462870.1:n.*372dup
NM_004531.4:c.*164dup	NP_004522.1:n.*164dup
NM_176806.3:c.*651dup	NP_789776.1:n.*651dup
NM_004531.5:c.*164dup MANE Select	NP_004522.1:n.*164dup
NM_176806.4:c.*651dup MANE Plus Clinical	NP_789776.1:n.*651dup