Canonical Allele Identifier: CA2215863941
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845369G= , CM000678.2:g.28845369G= GRCh38
NC_000016.9:g.28856690G= , CM000678.1:g.28856690G= GRCh37
NC_000016.8:g.28764191G= NCBI36
NG_008964.1:g.6040C=
NG_029706.2:g.3770G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.359C= MANE Select ENSP00000322439.3:p.Thr120=
ENST00000313511.7:c.359C= ENSP00000322439.3:p.Thr120=
ENST00000565012.1:c.248-314C= ENSP00000455007.1:n.248-314C=
NM_003321.4:c.359C= NP_003312.3:p.Thr120=
XM_011545928.1:c.359C= XP_011544230.1:p.Thr120=
NM_001365360.1:c.359C= NP_001352289.1:p.Thr120=
NM_003321.5:c.359C= MANE Select NP_003312.3:p.Thr120=
NM_001365360.2:c.359C= NP_001352289.1:p.Thr120=