Canonical Allele Identifier: CA2215863553
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845184_28845185delinsTG , CM000678.2:g.28845184_28845185delinsTG GRCh38
NC_000016.9:g.28856505_28856506delinsTG , CM000678.1:g.28856505_28856506delinsTG GRCh37
NC_000016.8:g.28764006_28764007delinsTG NCBI36
NG_008964.1:g.6224_6225delinsCA
NG_029706.2:g.3585_3586delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.415-130_415-129delinsCA MANE Select ENSP00000322439.3:n.415-130_415-129delinsCA
ENST00000313511.7:c.415-130_415-129delinsCA ENSP00000322439.3:n.415-130_415-129delinsCA
ENST00000565012.1:c.248-130_248-129delinsCA ENSP00000455007.1:n.248-130_248-129delinsCA
NM_003321.4:c.415-130_415-129delinsCA NP_003312.3:n.415-130_415-129delinsCA
XM_011545928.1:c.415-130_415-129delinsCA XP_011544230.1:n.415-130_415-129delinsCA
NM_001365360.1:c.415-130_415-129delinsCA NP_001352289.1:n.415-130_415-129delinsCA
NM_003321.5:c.415-130_415-129delinsCA MANE Select NP_003312.3:n.415-130_415-129delinsCA
NM_001365360.2:c.415-130_415-129delinsCA NP_001352289.1:n.415-130_415-129delinsCA