Canonical Allele Identifier: CA2215862877
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28844904C= , CM000678.2:g.28844904C= GRCh38
NC_000016.9:g.28856225C= , CM000678.1:g.28856225C= GRCh37
NC_000016.8:g.28763726C= NCBI36
NG_008964.1:g.6505G=
NG_029706.2:g.3305C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.520-42G= MANE Select ENSP00000322439.3:n.520-42G=
ENST00000313511.7:c.520-42G= ENSP00000322439.3:n.520-42G=
ENST00000561644.1:n.58-42G=
ENST00000565012.1:c.*47-42G= ENSP00000455007.1:n.*47-42G=
NM_003321.4:c.520-42G= NP_003312.3:n.520-42G=
XM_011545928.1:c.520-42G= XP_011544230.1:n.520-42G=
NM_001365360.1:c.520-42G= NP_001352289.1:n.520-42G=
NM_003321.5:c.520-42G= MANE Select NP_003312.3:n.520-42G=
NM_001365360.2:c.520-42G= NP_001352289.1:n.520-42G=