Canonical Allele Identifier: CA384021233

Gene: MGP C12orf60

Linked Data

• ClinVar Variation Id: 432101
• ClinVar RCV Id: RCV000497490
• dbSNP Id: rs1555094473
• MyVariant Identifiers: chr12:g.15038670C>T (hg19) ; chr12:g.14885736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14885736C>T , CM000674.2:g.14885736C>T	GRCh38
NC_000012.11:g.15038670C>T , CM000674.1:g.15038670C>T	GRCh37
NC_000012.10:g.14929937C>T	NCBI36
NG_023331.1:g.5184G>A
NG_023331.2:g.5184G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.56G>A (MGP) MANE Select	ENSP00000445907.1:p.Cys19Tyr
ENST00000648334.1:n.126-18271C>T (C12orf60)
ENST00000228938.5:c.56G>A (MGP)	ENSP00000228938.5:p.Cys19Tyr
ENST00000507170.2:n.119G>A (MGP)
ENST00000527783.1:n.76-13433C>T (C12orf60)
ENST00000533472.1:n.87-18271C>T (C12orf60)
ENST00000539261.5:c.56G>A (MGP)	ENSP00000445907.1:p.Cys19Tyr
ENST00000543822.1:n.21C>T (C12orf60)
NM_000900.3:c.56G>A (MGP)	NP_000891.2:p.Cys19Tyr
NM_001190839.1:c.56G>A (MGP)	NP_001177768.1:p.Cys19Tyr
NM_000900.4:c.56G>A (MGP)	NP_000891.2:p.Cys19Tyr
NM_001190839.2:c.56G>A (MGP)	NP_001177768.1:p.Cys19Tyr
NM_000900.5:c.56G>A (MGP) MANE Select	NP_000891.2:p.Cys19Tyr
NM_001190839.3:c.56G>A (MGP)	NP_001177768.1:p.Cys19Tyr