Canonical Allele Identifier: CA494484884
Gene: TUFM HGNC NCBI

Linked Data

dbSNP Id: rs1486247546

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845410A>G , CM000678.2:g.28845410A>G GRCh38
NC_000016.9:g.28856731A>G , CM000678.1:g.28856731A>G GRCh37
NC_000016.8:g.28764232A>G NCBI36
NG_008964.1:g.5999T>C
NG_029706.2:g.3811A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313511.8:c.318T>C MANE Select ENSP00000322439.3:p.Ala106=
ENST00000313511.7:c.318T>C ENSP00000322439.3:p.Ala106=
ENST00000565012.1:c.248-355T>C ENSP00000455007.1:n.248-355T>C
NM_003321.4:c.318T>C NP_003312.3:p.Ala106=
XM_011545928.1:c.318T>C XP_011544230.1:p.Ala106=
NM_001365360.1:c.318T>C NP_001352289.1:p.Ala106=
NM_003321.5:c.318T>C MANE Select NP_003312.3:p.Ala106=
NM_001365360.2:c.318T>C NP_001352289.1:p.Ala106=