Canonical Allele Identifier: CA395417999
Gene: TUFM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845325C>G , CM000678.2:g.28845325C>G GRCh38
NC_000016.9:g.28856646C>G , CM000678.1:g.28856646C>G GRCh37
NC_000016.8:g.28764147C>G NCBI36
NG_008964.1:g.6084G>C
NG_029706.2:g.3726C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313511.8:c.403G>C MANE Select ENSP00000322439.3:p.Asp135His
ENST00000313511.7:c.403G>C ENSP00000322439.3:p.Asp135His
ENST00000565012.1:c.248-270G>C ENSP00000455007.1:n.248-270G>C
NM_003321.4:c.403G>C NP_003312.3:p.Asp135His
XM_011545928.1:c.403G>C XP_011544230.1:p.Asp135His
NM_001365360.1:c.403G>C NP_001352289.1:p.Asp135His
NM_003321.5:c.403G>C MANE Select NP_003312.3:p.Asp135His
NM_001365360.2:c.403G>C NP_001352289.1:p.Asp135His