Canonical Allele Identifier: CA359693948

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52403046G>T (hg19) ; chr5:g.53107216G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53107216G>T , CM000667.2:g.53107216G>T	GRCh38
NC_000005.9:g.52403046G>T , CM000667.1:g.52403046G>T	GRCh37
NC_000005.8:g.52438803G>T	NCBI36
NG_008435.2:g.7553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.-42C>A MANE Select	ENSP00000380157.3:n.-42C>A
ENST00000450852.8:c.146C>A MANE Plus Clinical	ENSP00000411022.3:p.Ala49Asp
ENST00000361377.8:c.146C>A	ENSP00000355160.4:p.Ala49Asp
ENST00000396954.7:c.-42C>A	ENSP00000380157.3:n.-42C>A
ENST00000450852.7:c.146C>A	ENSP00000411022.3:p.Ala49Asp
ENST00000502402.5:n.882C>A
ENST00000508922.5:c.146C>A	ENSP00000426274.1:p.Ala49Asp
ENST00000510818.6:c.146C>A	ENSP00000424267.2:p.Ala49Asp
ENST00000514553.2:n.144C>A
ENST00000527216.5:c.131C>A	ENSP00000435326.1:p.Ala44Asp
ENST00000582677.5:c.146C>A	ENSP00000462870.1:p.Ala49Asp
ENST00000584946.5:c.146C>A	ENSP00000464663.1:p.Ala49Asp
NM_004531.4:c.-42C>A	NP_004522.1:n.-42C>A
NM_176806.3:c.146C>A	NP_789776.1:p.Ala49Asp
NM_004531.5:c.-42C>A MANE Select	NP_004522.1:n.-42C>A
NM_176806.4:c.146C>A MANE Plus Clinical	NP_789776.1:p.Ala49Asp