Canonical Allele Identifier: CA359692536

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52394433T>G (hg19) ; chr5:g.53098603T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098603T>G , CM000667.2:g.53098603T>G	GRCh38
NC_000005.9:g.52394433T>G , CM000667.1:g.52394433T>G	GRCh37
NC_000005.8:g.52430190T>G	NCBI36
NG_008435.2:g.16166A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.566A>C MANE Select	ENSP00000380157.3:p.Ter189Ser
ENST00000450852.8:c.*486A>C MANE Plus Clinical	ENSP00000411022.3:n.*486A>C
ENST00000361377.8:c.*335A>C	ENSP00000355160.4:n.*335A>C
ENST00000396954.7:c.566A>C	ENSP00000380157.3:p.Ter189Ser
ENST00000450852.7:c.*486A>C	ENSP00000411022.3:n.*486A>C
ENST00000502402.5:n.2313A>C
ENST00000508922.5:c.*406A>C	ENSP00000426274.1:n.*406A>C
ENST00000510818.6:c.*439A>C	ENSP00000424267.2:n.*439A>C
ENST00000582677.5:c.*207A>C	ENSP00000462870.1:n.*207A>C
ENST00000584946.5:c.*358A>C	ENSP00000464663.1:n.*358A>C
NM_004531.4:c.566A>C	NP_004522.1:p.Ter189Ser
NM_176806.3:c.*486A>C	NP_789776.1:n.*486A>C
NM_004531.5:c.566A>C MANE Select	NP_004522.1:p.Ter189Ser
NM_176806.4:c.*486A>C MANE Plus Clinical	NP_789776.1:n.*486A>C