Canonical Allele Identifier: CA2215863273
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845035T= , CM000678.2:g.28845035T= GRCh38
NC_000016.9:g.28856356T= , CM000678.1:g.28856356T= GRCh37
NC_000016.8:g.28763857T= NCBI36
NG_008964.1:g.6374A=
NG_029706.2:g.3436T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.435A= MANE Select ENSP00000322439.3:p.Ala145=
ENST00000313511.7:c.435A= ENSP00000322439.3:p.Ala145=
ENST00000565012.1:c.268A= ENSP00000455007.1:p.Thr90=
NM_003321.4:c.435A= NP_003312.3:p.Ala145=
XM_011545928.1:c.435A= XP_011544230.1:p.Ala145=
NM_001365360.1:c.435A= NP_001352289.1:p.Ala145=
NM_003321.5:c.435A= MANE Select NP_003312.3:p.Ala145=
NM_001365360.2:c.435A= NP_001352289.1:p.Ala145=