Canonical Allele Identifier: CA7985622
Gene: TUFM HGNC NCBI

Linked Data

dbSNP Id: rs750730381

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28844958G>A , CM000678.2:g.28844958G>A GRCh38
NC_000016.9:g.28856279G>A , CM000678.1:g.28856279G>A GRCh37
NC_000016.8:g.28763780G>A NCBI36
NG_008964.1:g.6451C>T
NG_029706.2:g.3359G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.512C>T MANE Select ENSP00000322439.3:p.Ala171Val
ENST00000313511.7:c.512C>T ENSP00000322439.3:p.Ala171Val
ENST00000561644.1:n.50C>T
ENST00000565012.1:c.*39C>T ENSP00000455007.1:n.*39C>T
NM_003321.4:c.512C>T NP_003312.3:p.Ala171Val
XM_011545928.1:c.512C>T XP_011544230.1:p.Ala171Val
NM_001365360.1:c.512C>T NP_001352289.1:p.Ala171Val
NM_003321.5:c.512C>T MANE Select NP_003312.3:p.Ala171Val
NM_001365360.2:c.512C>T NP_001352289.1:p.Ala171Val