Canonical Allele Identifier: CA392863607

Gene: MTFMT

Linked Data

• gnomAD v4: 15-65029579-G-C
• MyVariant Identifiers: chr15:g.65321917G>C (hg19) ; chr15:g.65029579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029579G>C , CM000677.2:g.65029579G>C	GRCh38
NC_000015.9:g.65321917G>C , CM000677.1:g.65321917G>C	GRCh37
NC_000015.8:g.63108970G>C	NCBI36
NG_029184.1:g.5061C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220058.9:c.35C>G MANE Select	ENSP00000220058.4:p.Pro12Arg
ENST00000220058.8:c.35C>G	ENSP00000220058.4:p.Pro12Arg
ENST00000543678.1:c.35C>G	ENSP00000443754.1:p.Pro12Arg
ENST00000558460.5:c.35C>G	ENSP00000452646.1:p.Pro12Arg
ENST00000560717.5:c.20C>G	ENSP00000457257.1:p.Pro7Arg
NM_139242.3:c.35C>G	NP_640335.2:p.Pro12Arg
XM_005254158.5:c.35C>G	XP_005254215.2:p.Pro12Arg
XR_001751081.1:n.50C>G
NM_139242.4:c.35C>G MANE Select	NP_640335.2:p.Pro12Arg