Canonical Allele Identifier: CA233311552

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14883341A>G , CM000674.2:g.14883341A>G	GRCh38
NC_000012.11:g.15036275A>G , CM000674.1:g.15036275A>G	GRCh37
NC_000012.10:g.14927542A>G	NCBI36
NG_023331.1:g.7579T>C
NG_023331.2:g.7579T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.95-294T>C (MGP) MANE Select	ENSP00000445907.1:n.95-294T>C
ENST00000648334.1:n.126-20666A>G (C12orf60)
ENST00000228938.5:c.170-294T>C (MGP)	ENSP00000228938.5:n.170-294T>C
ENST00000507170.2:n.1029T>C (MGP)
ENST00000527783.1:n.76-15828A>G (C12orf60)
ENST00000533472.1:n.87-20666A>G (C12orf60)
ENST00000539261.5:c.95-294T>C (MGP)	ENSP00000445907.1:n.95-294T>C
ENST00000545199.5:c.33+872T>C (MGP)
NM_000900.3:c.95-294T>C (MGP)	NP_000891.2:n.95-294T>C
NM_001190839.1:c.170-294T>C (MGP)	NP_001177768.1:n.170-294T>C
NM_000900.4:c.95-294T>C (MGP)	NP_000891.2:n.95-294T>C
NM_001190839.2:c.170-294T>C (MGP)	NP_001177768.1:n.170-294T>C
NM_000900.5:c.95-294T>C (MGP) MANE Select	NP_000891.2:n.95-294T>C
NM_001190839.3:c.170-294T>C (MGP)	NP_001177768.1:n.170-294T>C