Canonical Allele Identifier: CA359692577

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52394451A>T (hg19) ; chr5:g.53098621A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098621A>T , CM000667.2:g.53098621A>T	GRCh38
NC_000005.9:g.52394451A>T , CM000667.1:g.52394451A>T	GRCh37
NC_000005.8:g.52430208A>T	NCBI36
NG_008435.2:g.16148T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.548T>A MANE Select	ENSP00000380157.3:p.Phe183Tyr
ENST00000450852.8:c.*468T>A MANE Plus Clinical	ENSP00000411022.3:n.*468T>A
ENST00000361377.8:c.*317T>A	ENSP00000355160.4:n.*317T>A
ENST00000396954.7:c.548T>A	ENSP00000380157.3:p.Phe183Tyr
ENST00000450852.7:c.*468T>A	ENSP00000411022.3:n.*468T>A
ENST00000502402.5:n.2295T>A
ENST00000508922.5:c.*388T>A	ENSP00000426274.1:n.*388T>A
ENST00000510818.6:c.*421T>A	ENSP00000424267.2:n.*421T>A
ENST00000582677.5:c.*189T>A	ENSP00000462870.1:n.*189T>A
ENST00000584946.5:c.*340T>A	ENSP00000464663.1:n.*340T>A
NM_004531.4:c.548T>A	NP_004522.1:p.Phe183Tyr
NM_176806.3:c.*468T>A	NP_789776.1:n.*468T>A
NM_004531.5:c.548T>A MANE Select	NP_004522.1:p.Phe183Tyr
NM_176806.4:c.*468T>A MANE Plus Clinical	NP_789776.1:n.*468T>A