Canonical Allele Identifier: CA490824196
Gene: MTFMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.65298470A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65006132A>G , CM000677.2:g.65006132A>G GRCh38
NC_000015.9:g.65298470A>G , CM000677.1:g.65298470A>G GRCh37
NC_000015.8:g.63085523A>G NCBI36
NG_029184.1:g.28508T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220058.9:c.873T>C MANE Select ENSP00000220058.4:p.Val291=
ENST00000220058.8:c.873T>C ENSP00000220058.4:p.Val291=
ENST00000558460.5:c.873T>C ENSP00000452646.1:p.Val291=
ENST00000560717.5:c.748T>C ENSP00000457257.1:n.748T>C
NM_139242.3:c.873T>C NP_640335.2:p.Val291=
XM_005254158.3:c.618T>C XP_005254215.1:p.Val206=
XM_005254158.5:c.1026T>C XP_005254215.2:p.Val342=
NM_139242.4:c.873T>C MANE Select NP_640335.2:p.Val291=