Canonical Allele Identifier: CA2215863059
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28844981C= , CM000678.2:g.28844981C= GRCh38
NC_000016.9:g.28856302C= , CM000678.1:g.28856302C= GRCh37
NC_000016.8:g.28763803C= NCBI36
NG_008964.1:g.6428G=
NG_029706.2:g.3382C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.489G= MANE Select ENSP00000322439.3:p.Gln163=
ENST00000313511.7:c.489G= ENSP00000322439.3:p.Gln163=
ENST00000561644.1:n.27G=
ENST00000565012.1:c.*16G= ENSP00000455007.1:n.*16G=
NM_003321.4:c.489G= NP_003312.3:p.Gln163=
XM_011545928.1:c.489G= XP_011544230.1:p.Gln163=
NM_001365360.1:c.489G= NP_001352289.1:p.Gln163=
NM_003321.5:c.489G= MANE Select NP_003312.3:p.Gln163=
NM_001365360.2:c.489G= NP_001352289.1:p.Gln163=