Canonical Allele Identifier: CA2840828827
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845221dup , CM000678.2:g.28845221dup GRCh38
NC_000016.9:g.28856542dup , CM000678.1:g.28856542dup GRCh37
NC_000016.8:g.28764043dup NCBI36
NG_008964.1:g.6188dup
NG_029706.2:g.3622dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.414+93dup MANE Select ENSP00000322439.3:n.414+93dup
ENST00000313511.7:c.414+93dup ENSP00000322439.3:n.414+93dup
ENST00000565012.1:c.248-166dup ENSP00000455007.1:n.248-166dup
NM_003321.4:c.414+93dup NP_003312.3:n.414+93dup
XM_011545928.1:c.414+93dup XP_011544230.1:n.414+93dup
NM_001365360.1:c.414+93dup NP_001352289.1:n.414+93dup
NM_003321.5:c.414+93dup MANE Select NP_003312.3:n.414+93dup
NM_001365360.2:c.414+93dup NP_001352289.1:n.414+93dup