Canonical Allele Identifier: CA6465119

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882155C>T , CM000674.2:g.14882155C>T	GRCh38
NC_000012.11:g.15035089C>T , CM000674.1:g.15035089C>T	GRCh37
NC_000012.10:g.14926356C>T	NCBI36
NG_023331.1:g.8765G>A
NG_023331.2:g.8765G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.296G>A (MGP) MANE Select	ENSP00000445907.1:p.Arg99His
ENST00000648334.1:n.126-21852C>T (C12orf60)
ENST00000228938.5:c.371G>A (MGP)	ENSP00000228938.5:p.Arg124His
ENST00000527783.1:n.76-17014C>T (C12orf60)
ENST00000533472.1:n.87-21852C>T (C12orf60)
ENST00000539261.5:c.296G>A (MGP)	ENSP00000445907.1:p.Arg99His
ENST00000545199.5:c.159G>A (MGP)
NM_000900.3:c.296G>A (MGP)	NP_000891.2:p.Arg99His
NM_001190839.1:c.371G>A (MGP)	NP_001177768.1:p.Arg124His
NM_000900.4:c.296G>A (MGP)	NP_000891.2:p.Arg99His
NM_001190839.2:c.371G>A (MGP)	NP_001177768.1:p.Arg124His
NM_000900.5:c.296G>A (MGP) MANE Select	NP_000891.2:p.Arg99His
NM_001190839.3:c.371G>A (MGP)	NP_001177768.1:p.Arg124His