Canonical Allele Identifier: CA359693798

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52402980A>T (hg19) ; chr5:g.53107150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107150A>T , CM000667.2:g.53107150A>T	GRCh38
NC_000005.9:g.52402980A>T , CM000667.1:g.52402980A>T	GRCh37
NC_000005.8:g.52438737A>T	NCBI36
NG_008435.2:g.7619T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.25T>A MANE Select	ENSP00000380157.3:p.Ser9Thr
ENST00000450852.8:c.212T>A MANE Plus Clinical	ENSP00000411022.3:p.Leu71His
ENST00000361377.8:c.212T>A	ENSP00000355160.4:p.Leu71His
ENST00000396954.7:c.25T>A	ENSP00000380157.3:p.Ser9Thr
ENST00000450852.7:c.212T>A	ENSP00000411022.3:p.Leu71His
ENST00000502402.5:n.948T>A
ENST00000508922.5:c.212T>A	ENSP00000426274.1:p.Leu71His
ENST00000510818.6:c.212T>A	ENSP00000424267.2:p.Leu71His
ENST00000514553.2:n.210T>A
ENST00000527216.5:c.197T>A	ENSP00000435326.1:p.Leu66His
ENST00000582677.5:c.212T>A	ENSP00000462870.1:p.Leu71His
ENST00000584946.5:c.212T>A	ENSP00000464663.1:p.Leu71His
NM_004531.4:c.25T>A	NP_004522.1:p.Ser9Thr
NM_176806.3:c.212T>A	NP_789776.1:p.Leu71His
NM_004531.5:c.25T>A MANE Select	NP_004522.1:p.Ser9Thr
NM_176806.4:c.212T>A MANE Plus Clinical	NP_789776.1:p.Leu71His