Canonical Allele Identifier: CA2215863208
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845009A= , CM000678.2:g.28845009A= GRCh38
NC_000016.9:g.28856330A= , CM000678.1:g.28856330A= GRCh37
NC_000016.8:g.28763831A= NCBI36
NG_008964.1:g.6400T=
NG_029706.2:g.3410A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.461T= MANE Select ENSP00000322439.3:p.Val154=
ENST00000313511.7:c.461T= ENSP00000322439.3:p.Val154=
ENST00000565012.1:c.294T= ENSP00000455007.1:p.Gly98=
NM_003321.4:c.461T= NP_003312.3:p.Val154=
XM_011545928.1:c.461T= XP_011544230.1:p.Val154=
NM_001365360.1:c.461T= NP_001352289.1:p.Val154=
NM_003321.5:c.461T= MANE Select NP_003312.3:p.Val154=
NM_001365360.2:c.461T= NP_001352289.1:p.Val154=