Canonical Allele Identifier: CA2215864528
Gene: TUFM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845590T= , CM000678.2:g.28845590T= GRCh38
NC_000016.9:g.28856911T= , CM000678.1:g.28856911T= GRCh37
NC_000016.8:g.28764412T= NCBI36
NG_008964.1:g.5819A=
NG_029706.2:g.3991T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.248-110A= MANE Select ENSP00000322439.3:n.248-110A=
ENST00000313511.7:c.248-110A= ENSP00000322439.3:n.248-110A=
ENST00000565012.1:c.247+322A= ENSP00000455007.1:n.247+322A=
NM_003321.4:c.248-110A= NP_003312.3:n.248-110A=
XM_011545928.1:c.248-110A= XP_011544230.1:n.248-110A=
NM_001365360.1:c.248-110A= NP_001352289.1:n.248-110A=
NM_003321.5:c.248-110A= MANE Select NP_003312.3:n.248-110A=
NM_001365360.2:c.248-110A= NP_001352289.1:n.248-110A=
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