Canonical Allele Identifier: CA2215863026
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28844975T= , CM000678.2:g.28844975T= GRCh38
NC_000016.9:g.28856296T= , CM000678.1:g.28856296T= GRCh37
NC_000016.8:g.28763797T= NCBI36
NG_008964.1:g.6434A=
NG_029706.2:g.3376T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.495A= MANE Select ENSP00000322439.3:p.Arg165=
ENST00000313511.7:c.495A= ENSP00000322439.3:p.Arg165=
ENST00000561644.1:n.33A=
ENST00000565012.1:c.*22A= ENSP00000455007.1:n.*22A=
NM_003321.4:c.495A= NP_003312.3:p.Arg165=
XM_011545928.1:c.495A= XP_011544230.1:p.Arg165=
NM_001365360.1:c.495A= NP_001352289.1:p.Arg165=
NM_003321.5:c.495A= MANE Select NP_003312.3:p.Arg165=
NM_001365360.2:c.495A= NP_001352289.1:p.Arg165=