Canonical Allele Identifier: CA490824195
Gene: MTFMT HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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