Canonical Allele Identifier: CA494484890
Gene: TUFM HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.28856737C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845416C>T , CM000678.2:g.28845416C>T GRCh38
NC_000016.9:g.28856737C>T , CM000678.1:g.28856737C>T GRCh37
NC_000016.8:g.28764238C>T NCBI36
NG_008964.1:g.5993G>A
NG_029706.2:g.3817C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000313511.8:c.312G>A MANE Select ENSP00000322439.3:p.Glu104=
ENST00000313511.7:c.312G>A ENSP00000322439.3:p.Glu104=
ENST00000565012.1:c.248-361G>A ENSP00000455007.1:n.248-361G>A
NM_003321.4:c.312G>A NP_003312.3:p.Glu104=
XM_011545928.1:c.312G>A XP_011544230.1:p.Glu104=
NM_001365360.1:c.312G>A NP_001352289.1:p.Glu104=
NM_003321.5:c.312G>A MANE Select NP_003312.3:p.Glu104=
NM_001365360.2:c.312G>A NP_001352289.1:p.Glu104=