Canonical Allele Identifier: CA2215863393
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845103_28845104delinsGT , CM000678.2:g.28845103_28845104delinsGT GRCh38
NC_000016.9:g.28856424_28856425delinsGT , CM000678.1:g.28856424_28856425delinsGT GRCh37
NC_000016.8:g.28763925_28763926delinsGT NCBI36
NG_008964.1:g.6305_6306delinsAC
NG_029706.2:g.3504_3505delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.415-49_415-48delinsAC MANE Select ENSP00000322439.3:n.415-49_415-48delinsAC
ENST00000313511.7:c.415-49_415-48delinsAC ENSP00000322439.3:n.415-49_415-48delinsAC
ENST00000565012.1:c.248-49_248-48delinsAC ENSP00000455007.1:n.248-49_248-48delinsAC
NM_003321.4:c.415-49_415-48delinsAC NP_003312.3:n.415-49_415-48delinsAC
XM_011545928.1:c.415-49_415-48delinsAC XP_011544230.1:n.415-49_415-48delinsAC
NM_001365360.1:c.415-49_415-48delinsAC NP_001352289.1:n.415-49_415-48delinsAC
NM_003321.5:c.415-49_415-48delinsAC MANE Select NP_003312.3:n.415-49_415-48delinsAC
NM_001365360.2:c.415-49_415-48delinsAC NP_001352289.1:n.415-49_415-48delinsAC