Canonical Allele Identifier: CA2215863787
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845313C= , CM000678.2:g.28845313C= GRCh38
NC_000016.9:g.28856634C= , CM000678.1:g.28856634C= GRCh37
NC_000016.8:g.28764135C= NCBI36
NG_008964.1:g.6096G=
NG_029706.2:g.3714C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.414+1G= MANE Select ENSP00000322439.3:n.414+1G=
ENST00000313511.7:c.414+1G= ENSP00000322439.3:n.414+1G=
ENST00000565012.1:c.248-258G= ENSP00000455007.1:n.248-258G=
NM_003321.4:c.414+1G= NP_003312.3:n.414+1G=
XM_011545928.1:c.414+1G= XP_011544230.1:n.414+1G=
NM_001365360.1:c.414+1G= NP_001352289.1:n.414+1G=
NM_003321.5:c.414+1G= MANE Select NP_003312.3:n.414+1G=
NM_001365360.2:c.414+1G= NP_001352289.1:n.414+1G=