Canonical Allele Identifier: CA494484788
Gene: TUFM HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.28856326T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845005T>G , CM000678.2:g.28845005T>G GRCh38
NC_000016.9:g.28856326T>G , CM000678.1:g.28856326T>G GRCh37
NC_000016.8:g.28763827T>G NCBI36
NG_008964.1:g.6404A>C
NG_029706.2:g.3406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.465A>C MANE Select ENSP00000322439.3:p.Ala155=
ENST00000313511.7:c.465A>C ENSP00000322439.3:p.Ala155=
ENST00000561644.1:n.3A>C
ENST00000565012.1:c.298A>C ENSP00000455007.1:p.Ser100Arg
NM_003321.4:c.465A>C NP_003312.3:p.Ala155=
XM_011545928.1:c.465A>C XP_011544230.1:p.Ala155=
NM_001365360.1:c.465A>C NP_001352289.1:p.Ala155=
NM_003321.5:c.465A>C MANE Select NP_003312.3:p.Ala155=
NM_001365360.2:c.465A>C NP_001352289.1:p.Ala155=
Search 100 bp 5'
Search 100 bp 3'