Canonical Allele Identifier: CA444164215

Gene: MOCS2

Linked Data

• MyVariant Identifiers: chr5:g.52394429T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098599T>G , CM000667.2:g.53098599T>G	GRCh38
NC_000005.9:g.52394429T>G , CM000667.1:g.52394429T>G	GRCh37
NC_000005.8:g.52430186T>G	NCBI36
NG_008435.2:g.16170A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*3A>C MANE Select	ENSP00000380157.3:n.*3A>C
ENST00000450852.8:c.*490A>C MANE Plus Clinical	ENSP00000411022.3:n.*490A>C
ENST00000361377.8:c.*339A>C	ENSP00000355160.4:n.*339A>C
ENST00000396954.7:c.*3A>C	ENSP00000380157.3:n.*3A>C
ENST00000450852.7:c.*490A>C	ENSP00000411022.3:n.*490A>C
ENST00000502402.5:n.2317A>C
ENST00000508922.5:c.*410A>C	ENSP00000426274.1:n.*410A>C
ENST00000510818.6:c.*443A>C	ENSP00000424267.2:n.*443A>C
ENST00000582677.5:c.*211A>C	ENSP00000462870.1:n.*211A>C
ENST00000584946.5:c.*362A>C	ENSP00000464663.1:n.*362A>C
NM_004531.4:c.*3A>C	NP_004522.1:n.*3A>C
NM_176806.3:c.*490A>C	NP_789776.1:n.*490A>C
NM_004531.5:c.*3A>C MANE Select	NP_004522.1:n.*3A>C
NM_176806.4:c.*490A>C MANE Plus Clinical	NP_789776.1:n.*490A>C