Canonical Allele Identifier: CA359692620

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52394469T>C (hg19) ; chr5:g.53098639T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098639T>C , CM000667.2:g.53098639T>C	GRCh38
NC_000005.9:g.52394469T>C , CM000667.1:g.52394469T>C	GRCh37
NC_000005.8:g.52430226T>C	NCBI36
NG_008435.2:g.16130A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.530A>G MANE Select	ENSP00000380157.3:p.Lys177Arg
ENST00000450852.8:c.*450A>G MANE Plus Clinical	ENSP00000411022.3:n.*450A>G
ENST00000361377.8:c.*299A>G	ENSP00000355160.4:n.*299A>G
ENST00000396954.7:c.530A>G	ENSP00000380157.3:p.Lys177Arg
ENST00000450852.7:c.*450A>G	ENSP00000411022.3:n.*450A>G
ENST00000502402.5:n.2277A>G
ENST00000508922.5:c.*370A>G	ENSP00000426274.1:n.*370A>G
ENST00000510818.6:c.*403A>G	ENSP00000424267.2:n.*403A>G
ENST00000582677.5:c.*171A>G	ENSP00000462870.1:n.*171A>G
ENST00000584946.5:c.*322A>G	ENSP00000464663.1:n.*322A>G
NM_004531.4:c.530A>G	NP_004522.1:p.Lys177Arg
NM_176806.3:c.*450A>G	NP_789776.1:n.*450A>G
NM_004531.5:c.530A>G MANE Select	NP_004522.1:p.Lys177Arg
NM_176806.4:c.*450A>G MANE Plus Clinical	NP_789776.1:n.*450A>G