Canonical Allele Identifier: CA13614802

Gene: MGP C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14882575G>A , CM000674.2:g.14882575G>A	GRCh38
NC_000012.11:g.15035509G>A , CM000674.1:g.15035509G>A	GRCh37
NC_000012.10:g.14926776G>A	NCBI36
NG_023331.1:g.8345C>T
NG_023331.2:g.8345C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539261.6:c.171-295C>T (MGP) MANE Select	ENSP00000445907.1:n.171-295C>T
ENST00000648334.1:n.126-21432G>A (C12orf60)
ENST00000228938.5:c.246-295C>T (MGP)	ENSP00000228938.5:n.246-295C>T
ENST00000527783.1:n.76-16594G>A (C12orf60)
ENST00000533472.1:n.87-21432G>A (C12orf60)
ENST00000539261.5:c.171-295C>T (MGP)	ENSP00000445907.1:n.171-295C>T
ENST00000545199.5:c.34-295C>T (MGP)
NM_000900.3:c.171-295C>T (MGP)	NP_000891.2:n.171-295C>T
NM_001190839.1:c.246-295C>T (MGP)	NP_001177768.1:n.246-295C>T
NM_000900.4:c.171-295C>T (MGP)	NP_000891.2:n.171-295C>T
NM_001190839.2:c.246-295C>T (MGP)	NP_001177768.1:n.246-295C>T
NM_000900.5:c.171-295C>T (MGP) MANE Select	NP_000891.2:n.171-295C>T
NM_001190839.3:c.246-295C>T (MGP)	NP_001177768.1:n.246-295C>T