Canonical Allele Identifier: CA2215863641
Gene: TUFM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845248A= , CM000678.2:g.28845248A= GRCh38
NC_000016.9:g.28856569A= , CM000678.1:g.28856569A= GRCh37
NC_000016.8:g.28764070A= NCBI36
NG_008964.1:g.6161T=
NG_029706.2:g.3649A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.414+66T= MANE Select ENSP00000322439.3:n.414+66T=
ENST00000313511.7:c.414+66T= ENSP00000322439.3:n.414+66T=
ENST00000565012.1:c.248-193T= ENSP00000455007.1:n.248-193T=
NM_003321.4:c.414+66T= NP_003312.3:n.414+66T=
XM_011545928.1:c.414+66T= XP_011544230.1:n.414+66T=
NM_001365360.1:c.414+66T= NP_001352289.1:n.414+66T=
NM_003321.5:c.414+66T= MANE Select NP_003312.3:n.414+66T=
NM_001365360.2:c.414+66T= NP_001352289.1:n.414+66T=
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