Canonical Allele Identifier: CA2215863654
Gene: TUFM HGNC NCBI

Linked Data

dbSNP Id: rs1961910262

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845254_28845256del , CM000678.2:g.28845254_28845256del GRCh38
NC_000016.9:g.28856575_28856577del , CM000678.1:g.28856575_28856577del GRCh37
NC_000016.8:g.28764076_28764078del NCBI36
NG_008964.1:g.6154_6156del
NG_029706.2:g.3655_3657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.414+59_414+61del MANE Select ENSP00000322439.3:n.414+59_414+61del
ENST00000313511.7:c.414+59_414+61del ENSP00000322439.3:n.414+59_414+61del
ENST00000565012.1:c.248-200_248-198del ENSP00000455007.1:n.248-200_248-198del
NM_003321.4:c.414+59_414+61del NP_003312.3:n.414+59_414+61del
XM_011545928.1:c.414+59_414+61del XP_011544230.1:n.414+59_414+61del
NM_001365360.1:c.414+59_414+61del NP_001352289.1:n.414+59_414+61del
NM_003321.5:c.414+59_414+61del MANE Select NP_003312.3:n.414+59_414+61del
NM_001365360.2:c.414+59_414+61del NP_001352289.1:n.414+59_414+61del