Canonical Allele Identifier: CA2215864018
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845400T= , CM000678.2:g.28845400T= GRCh38
NC_000016.9:g.28856721T= , CM000678.1:g.28856721T= GRCh37
NC_000016.8:g.28764222T= NCBI36
NG_008964.1:g.6009A=
NG_029706.2:g.3801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.328A= MANE Select ENSP00000322439.3:p.Thr110=
ENST00000313511.7:c.328A= ENSP00000322439.3:p.Thr110=
ENST00000565012.1:c.248-345A= ENSP00000455007.1:n.248-345A=
NM_003321.4:c.328A= NP_003312.3:p.Thr110=
XM_011545928.1:c.328A= XP_011544230.1:p.Thr110=
NM_001365360.1:c.328A= NP_001352289.1:p.Thr110=
NM_003321.5:c.328A= MANE Select NP_003312.3:p.Thr110=
NM_001365360.2:c.328A= NP_001352289.1:p.Thr110=