Canonical Allele Identifier: CA395418688
Gene: TUFM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845444T>A , CM000678.2:g.28845444T>A GRCh38
NC_000016.9:g.28856765T>A , CM000678.1:g.28856765T>A GRCh37
NC_000016.8:g.28764266T>A NCBI36
NG_008964.1:g.5965A>T
NG_029706.2:g.3845T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.284A>T MANE Select ENSP00000322439.3:p.Tyr95Phe
ENST00000313511.7:c.284A>T ENSP00000322439.3:p.Tyr95Phe
ENST00000565012.1:c.248-389A>T ENSP00000455007.1:n.248-389A>T
NM_003321.4:c.284A>T NP_003312.3:p.Tyr95Phe
XM_011545928.1:c.284A>T XP_011544230.1:p.Tyr95Phe
NM_001365360.1:c.284A>T NP_001352289.1:p.Tyr95Phe
NM_003321.5:c.284A>T MANE Select NP_003312.3:p.Tyr95Phe
NM_001365360.2:c.284A>T NP_001352289.1:p.Tyr95Phe