Canonical Allele Identifier: CA2200846335

Gene: MPG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81110C= , CM000678.2:g.81110C=	GRCh38
NC_000016.9:g.131109C= , CM000678.1:g.131109C=	GRCh37
NC_000016.8:g.71109C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001015052.3:c.300+1410C= MANE Select	NP_001015052.1:n.300+1410C=
ENST00000356432.8:c.300+1410C= MANE Select	ENSP00000348809.4:n.300+1410C=
NM_001015052.2:c.300+1410C=	NP_001015052.1:n.300+1410C=
NM_001015054.2:c.264+1410C=	NP_001015054.1:n.264+1410C=
NM_001015054.3:c.264+1410C=	NP_001015054.1:n.264+1410C=
NM_002434.3:c.315+1410C=	NP_002425.2:n.315+1410C=
NM_002434.4:c.315+1410C=	NP_002425.2:n.315+1410C=
ENST00000219431.4:c.315+1410C=	ENSP00000219431.4:n.315+1410C=
ENST00000356432.7:c.300+1410C=	ENSP00000348809.3:n.300+1410C=
ENST00000397817.5:c.264+1410C=	ENSP00000380918.1:n.264+1410C=
ENST00000436333.5:c.264+1410C=	ENSP00000388097.1:n.264+1410C=
XM_011522779.1:c.-381C=	XP_011521081.1:n.-381C=
XM_024450282.1:c.315+1410C=	XP_024306050.1:n.315+1410C=