Canonical Allele Identifier: CA359694184

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53108619T>G , CM000667.2:g.53108619T>G	GRCh38
NC_000005.9:g.52404449T>G , CM000667.1:g.52404449T>G	GRCh37
NC_000005.8:g.52440206T>G	NCBI36
NG_008435.2:g.6150A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004531.5:c.-145A>C MANE Select	NP_004522.1:n.-145A>C
ENST00000396954.8:c.-145A>C MANE Select	ENSP00000380157.3:n.-145A>C
NM_176806.4:c.43A>C MANE Plus Clinical	NP_789776.1:p.Ser15Arg
ENST00000450852.8:c.43A>C MANE Plus Clinical	ENSP00000411022.3:p.Ser15Arg
NM_004531.4:c.-145A>C	NP_004522.1:n.-145A>C
NM_176806.3:c.43A>C	NP_789776.1:p.Ser15Arg
ENST00000361377.8:c.43A>C	ENSP00000355160.4:p.Ser15Arg
ENST00000396954.7:c.-145A>C	ENSP00000380157.3:n.-145A>C
ENST00000450852.7:c.43A>C	ENSP00000411022.3:p.Ser15Arg
ENST00000508922.5:c.43A>C	ENSP00000426274.1:p.Ser15Arg
ENST00000510818.6:c.43A>C	ENSP00000424267.2:p.Ser15Arg
ENST00000514553.2:n.41A>C
ENST00000527216.5:c.28A>C	ENSP00000435326.1:p.Ser10Arg
ENST00000582677.5:c.43A>C	ENSP00000462870.1:p.Ser15Arg
ENST00000584946.5:c.43A>C	ENSP00000464663.1:p.Ser15Arg