Canonical Allele Identifier: CA490824198
Gene: MTFMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65298473T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65006135T>C , CM000677.2:g.65006135T>C GRCh38
NC_000015.9:g.65298473T>C , CM000677.1:g.65298473T>C GRCh37
NC_000015.8:g.63085526T>C NCBI36
NG_029184.1:g.28505A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.870A>G MANE Select ENSP00000220058.4:p.Glu290=
ENST00000220058.8:c.870A>G ENSP00000220058.4:p.Glu290=
ENST00000558460.5:c.870A>G ENSP00000452646.1:p.Glu290=
ENST00000560717.5:c.745A>G ENSP00000457257.1:n.745A>G
NM_139242.3:c.870A>G NP_640335.2:p.Glu290=
XM_005254158.3:c.615A>G XP_005254215.1:p.Glu205=
XM_005254158.5:c.1023A>G XP_005254215.2:p.Glu341=
NM_139242.4:c.870A>G MANE Select NP_640335.2:p.Glu290=