Canonical Allele Identifier: CA1946792978
Gene: MTG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133412251C= , CM000672.2:g.133412251C= GRCh38
NC_000010.10:g.135225755C= , CM000672.1:g.135225755C= GRCh37
NC_000010.9:g.135075745C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000317502.11:c.753-7229C= MANE Select ENSP00000323047.6:n.753-7229C=
ENST00000468317.3:c.*677-7229C= ENSP00000436767.2:n.*677-7229C=
ENST00000317502.10:c.753-7229C= ENSP00000323047.6:n.753-7229C=
ENST00000432508.3:c.600-7229C= ENSP00000393480.2:n.600-7229C=
ENST00000460848.5:n.1336-7229C=
ENST00000468317.2:c.768-7229C= ENSP00000436767.1:n.768-7229C=
ENST00000473735.1:n.1607-7229C=
ENST00000477902.6:c.630-7229C= ENSP00000475596.1:n.630-7229C=
NM_138384.2:c.753-7229C= NP_612393.2:n.753-7229C=
NM_138384.3:c.753-7229C= NP_612393.2:n.753-7229C=
NM_138384.4:c.753-7229C= MANE Select NP_612393.2:n.753-7229C=
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