Canonical Allele Identifier: CA1946792938

Gene: MTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133412187G= , CM000672.2:g.133412187G=	GRCh38
NC_000010.10:g.135225691G= , CM000672.1:g.135225691G=	GRCh37
NC_000010.9:g.135075681G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317502.11:c.753-7293G= MANE Select	ENSP00000323047.6:n.753-7293G=
ENST00000468317.3:c.*677-7293G=	ENSP00000436767.2:n.*677-7293G=
ENST00000317502.10:c.753-7293G=	ENSP00000323047.6:n.753-7293G=
ENST00000432508.3:c.600-7293G=	ENSP00000393480.2:n.600-7293G=
ENST00000460848.5:n.1336-7293G=
ENST00000468317.2:c.768-7293G=	ENSP00000436767.1:n.768-7293G=
ENST00000473735.1:n.1607-7293G=
ENST00000477902.6:c.630-7293G=	ENSP00000475596.1:n.630-7293G=
NM_138384.2:c.753-7293G=	NP_612393.2:n.753-7293G=
NM_138384.3:c.753-7293G=	NP_612393.2:n.753-7293G=
NM_138384.4:c.753-7293G= MANE Select	NP_612393.2:n.753-7293G=