Canonical Allele Identifier: CA233310840

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882708A>C , CM000674.2:g.14882708A>C	GRCh38
NC_000012.11:g.15035642A>C , CM000674.1:g.15035642A>C	GRCh37
NC_000012.10:g.14926909A>C	NCBI36
NG_023331.1:g.8212T>G
NG_023331.2:g.8212T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.170+264T>G (MGP) MANE Select	ENSP00000445907.1:n.170+264T>G
ENST00000648334.1:n.126-21299A>C (C12orf60)
ENST00000228938.5:c.245+264T>G (MGP)	ENSP00000228938.5:n.245+264T>G
ENST00000527783.1:n.76-16461A>C (C12orf60)
ENST00000533472.1:n.87-21299A>C (C12orf60)
ENST00000539261.5:c.170+264T>G (MGP)	ENSP00000445907.1:n.170+264T>G
ENST00000545199.5:c.34-428T>G (MGP)
NM_000900.3:c.170+264T>G (MGP)	NP_000891.2:n.170+264T>G
NM_001190839.1:c.245+264T>G (MGP)	NP_001177768.1:n.245+264T>G
NM_000900.4:c.170+264T>G (MGP)	NP_000891.2:n.170+264T>G
NM_001190839.2:c.245+264T>G (MGP)	NP_001177768.1:n.245+264T>G
NM_000900.5:c.170+264T>G (MGP) MANE Select	NP_000891.2:n.170+264T>G
NM_001190839.3:c.245+264T>G (MGP)	NP_001177768.1:n.245+264T>G