Canonical Allele Identifier: CA10641436

Gene: MGP C12orf60

Linked Data

• ClinVar Variation Id: 307765
• ClinVar RCV Id: RCV000395879
• dbSNP Id: rs886049104
• MyVariant Identifiers: chr12:g.15034758dupT (hg19) ; chr12:g.15034757_15034758insT (hg19) ; chr12:g.14881824dupT (hg38) ; chr12:g.14881823_14881824insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14881827dup , CM000674.2:g.14881827dup	GRCh38
NC_000012.11:g.15034761dup , CM000674.1:g.15034761dup	GRCh37
NC_000012.10:g.14926028dup	NCBI36
NG_023331.1:g.9096dup
NG_023331.2:g.9096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.*315dup (MGP) MANE Select	ENSP00000445907.1:n.*315dup
ENST00000648334.1:n.126-22180dup (C12orf60)
ENST00000527783.1:n.76-17342dup (C12orf60)
ENST00000533472.1:n.87-22180dup (C12orf60)
ENST00000539261.5:c.*315dup (MGP)	ENSP00000445907.1:n.*315dup
NM_000900.3:c.*315dup (MGP)	NP_000891.2:n.*315dup
NM_001190839.1:c.*315dup (MGP)	NP_001177768.1:n.*315dup
NM_000900.4:c.*315dup (MGP)	NP_000891.2:n.*315dup
NM_001190839.2:c.*315dup (MGP)	NP_001177768.1:n.*315dup
NM_000900.5:c.*315dup (MGP) MANE Select	NP_000891.2:n.*315dup
NM_001190839.3:c.*315dup (MGP)	NP_001177768.1:n.*315dup