Canonical Allele Identifier: CA6465138

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882225A>G , CM000674.2:g.14882225A>G	GRCh38
NC_000012.11:g.15035159A>G , CM000674.1:g.15035159A>G	GRCh37
NC_000012.10:g.14926426A>G	NCBI36
NG_023331.1:g.8695T>C
NG_023331.2:g.8695T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000900.5:c.226T>C (MGP) MANE Select	NP_000891.2:p.Tyr76His
ENST00000539261.6:c.226T>C (MGP) MANE Select	ENSP00000445907.1:p.Tyr76His
NM_000900.3:c.226T>C (MGP)	NP_000891.2:p.Tyr76His
NM_000900.4:c.226T>C (MGP)	NP_000891.2:p.Tyr76His
NM_001190839.1:c.301T>C (MGP)	NP_001177768.1:p.Tyr101His
NM_001190839.2:c.301T>C (MGP)	NP_001177768.1:p.Tyr101His
NM_001190839.3:c.301T>C (MGP)	NP_001177768.1:p.Tyr101His
ENST00000228938.5:c.301T>C (MGP)	ENSP00000228938.5:p.Tyr101His
ENST00000527783.1:n.76-16944A>G (C12orf60)
ENST00000533472.1:n.87-21782A>G (C12orf60)
ENST00000539261.5:c.226T>C (MGP)	ENSP00000445907.1:p.Tyr76His
ENST00000545199.5:c.89T>C (MGP)
ENST00000648334.1:n.126-21782A>G (C12orf60)