Canonical Allele Identifier: CA2215864538
Gene: TUFM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845601G= , CM000678.2:g.28845601G= GRCh38
NC_000016.9:g.28856922G= , CM000678.1:g.28856922G= GRCh37
NC_000016.8:g.28764423G= NCBI36
NG_008964.1:g.5808C=
NG_029706.2:g.4002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.248-121C= MANE Select ENSP00000322439.3:n.248-121C=
ENST00000313511.7:c.248-121C= ENSP00000322439.3:n.248-121C=
ENST00000565012.1:c.247+311C= ENSP00000455007.1:n.247+311C=
NM_003321.4:c.248-121C= NP_003312.3:n.248-121C=
XM_011545928.1:c.248-121C= XP_011544230.1:n.248-121C=
NM_001365360.1:c.248-121C= NP_001352289.1:n.248-121C=
NM_003321.5:c.248-121C= MANE Select NP_003312.3:n.248-121C=
NM_001365360.2:c.248-121C= NP_001352289.1:n.248-121C=
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