Canonical Allele Identifier: CA384019762

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882201T>A , CM000674.2:g.14882201T>A	GRCh38
NC_000012.11:g.15035135T>A , CM000674.1:g.15035135T>A	GRCh37
NC_000012.10:g.14926402T>A	NCBI36
NG_023331.1:g.8719A>T
NG_023331.2:g.8719A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000900.5:c.250A>T (MGP) MANE Select	NP_000891.2:p.Met84Leu
ENST00000539261.6:c.250A>T (MGP) MANE Select	ENSP00000445907.1:p.Met84Leu
NM_000900.3:c.250A>T (MGP)	NP_000891.2:p.Met84Leu
NM_000900.4:c.250A>T (MGP)	NP_000891.2:p.Met84Leu
NM_001190839.1:c.325A>T (MGP)	NP_001177768.1:p.Met109Leu
NM_001190839.2:c.325A>T (MGP)	NP_001177768.1:p.Met109Leu
NM_001190839.3:c.325A>T (MGP)	NP_001177768.1:p.Met109Leu
ENST00000228938.5:c.325A>T (MGP)	ENSP00000228938.5:p.Met109Leu
ENST00000527783.1:n.76-16968T>A (C12orf60)
ENST00000533472.1:n.87-21806T>A (C12orf60)
ENST00000539261.5:c.250A>T (MGP)	ENSP00000445907.1:p.Met84Leu
ENST00000545199.5:c.113A>T (MGP)
ENST00000648334.1:n.126-21806T>A (C12orf60)