Canonical Allele Identifier: CA2632531437
Gene: TUFM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845513A>G , CM000678.2:g.28845513A>G GRCh38
NC_000016.9:g.28856834A>G , CM000678.1:g.28856834A>G GRCh37
NC_000016.8:g.28764335A>G NCBI36
NG_008964.1:g.5896T>C
NG_029706.2:g.3914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.248-33T>C MANE Select ENSP00000322439.3:n.248-33T>C
ENST00000313511.7:c.248-33T>C ENSP00000322439.3:n.248-33T>C
ENST00000565012.1:c.247+399T>C ENSP00000455007.1:n.247+399T>C
NM_003321.4:c.248-33T>C NP_003312.3:n.248-33T>C
XM_011545928.1:c.248-33T>C XP_011544230.1:n.248-33T>C
NM_001365360.1:c.248-33T>C NP_001352289.1:n.248-33T>C
NM_003321.5:c.248-33T>C MANE Select NP_003312.3:n.248-33T>C
NM_001365360.2:c.248-33T>C NP_001352289.1:n.248-33T>C