Canonical Allele Identifier: CA7985625
Gene: TUFM HGNC NCBI

Linked Data

dbSNP Id: rs200563863

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28844976C>T , CM000678.2:g.28844976C>T GRCh38
NC_000016.9:g.28856297C>T , CM000678.1:g.28856297C>T GRCh37
NC_000016.8:g.28763798C>T NCBI36
NG_008964.1:g.6433G>A
NG_029706.2:g.3377C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.494G>A MANE Select ENSP00000322439.3:p.Arg165Gln
ENST00000313511.7:c.494G>A ENSP00000322439.3:p.Arg165Gln
ENST00000561644.1:n.32G>A
ENST00000565012.1:c.*21G>A ENSP00000455007.1:n.*21G>A
NM_003321.4:c.494G>A NP_003312.3:p.Arg165Gln
XM_011545928.1:c.494G>A XP_011544230.1:p.Arg165Gln
NM_001365360.1:c.494G>A NP_001352289.1:p.Arg165Gln
NM_003321.5:c.494G>A MANE Select NP_003312.3:p.Arg165Gln
NM_001365360.2:c.494G>A NP_001352289.1:p.Arg165Gln