Canonical Allele Identifier: CA2497029278

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882147T= , CM000674.2:g.14882147T=	GRCh38
NC_000012.11:g.15035081T= , CM000674.1:g.15035081T=	GRCh37
NC_000012.10:g.14926348T=	NCBI36
NG_023331.1:g.8773A=
NG_023331.2:g.8773A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.304A= (MGP) MANE Select	ENSP00000445907.1:p.Thr102=
ENST00000648334.1:n.126-21860T= (C12orf60)
ENST00000228938.5:c.379A= (MGP)	ENSP00000228938.5:p.Thr127=
ENST00000527783.1:n.76-17022T= (C12orf60)
ENST00000533472.1:n.87-21860T= (C12orf60)
ENST00000539261.5:c.304A= (MGP)	ENSP00000445907.1:p.Thr102=
ENST00000545199.5:c.167A= (MGP)
NM_000900.3:c.304A= (MGP)	NP_000891.2:p.Thr102=
NM_001190839.1:c.379A= (MGP)	NP_001177768.1:p.Thr127=
NM_000900.4:c.304A= (MGP)	NP_000891.2:p.Thr102=
NM_001190839.2:c.379A= (MGP)	NP_001177768.1:p.Thr127=
NM_000900.5:c.304A= (MGP) MANE Select	NP_000891.2:p.Thr102=
NM_001190839.3:c.379A= (MGP)	NP_001177768.1:p.Thr127=