Canonical Allele Identifier: CA2766471644

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098440_53098441dup , CM000667.2:g.53098440_53098441dup	GRCh38
NC_000005.9:g.52394270_52394271dup , CM000667.1:g.52394270_52394271dup	GRCh37
NC_000005.8:g.52430027_52430028dup	NCBI36
NG_008435.2:g.16328_16329dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*161_*162dup MANE Select	ENSP00000380157.3:n.*161_*162dup
ENST00000450852.8:c.*648_*649dup MANE Plus Clinical	ENSP00000411022.3:n.*648_*649dup
ENST00000361377.8:c.*497_*498dup	ENSP00000355160.4:n.*497_*498dup
ENST00000396954.7:c.*161_*162dup	ENSP00000380157.3:n.*161_*162dup
ENST00000450852.7:c.*648_*649dup	ENSP00000411022.3:n.*648_*649dup
ENST00000502402.5:n.2475_2476dup
ENST00000508922.5:c.*568_*569dup	ENSP00000426274.1:n.*568_*569dup
ENST00000510818.6:c.*601_*602dup	ENSP00000424267.2:n.*601_*602dup
ENST00000582677.5:c.*369_*370dup	ENSP00000462870.1:n.*369_*370dup
NM_004531.4:c.*161_*162dup	NP_004522.1:n.*161_*162dup
NM_176806.3:c.*648_*649dup	NP_789776.1:n.*648_*649dup
NM_004531.5:c.*161_*162dup MANE Select	NP_004522.1:n.*161_*162dup
NM_176806.4:c.*648_*649dup MANE Plus Clinical	NP_789776.1:n.*648_*649dup