Canonical Allele Identifier: CA395418192
Gene: TUFM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845353G>T , CM000678.2:g.28845353G>T GRCh38
NC_000016.9:g.28856674G>T , CM000678.1:g.28856674G>T GRCh37
NC_000016.8:g.28764175G>T NCBI36
NG_008964.1:g.6056C>A
NG_029706.2:g.3754G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.375C>A MANE Select ENSP00000322439.3:p.Tyr125Ter
ENST00000313511.7:c.375C>A ENSP00000322439.3:p.Tyr125Ter
ENST00000565012.1:c.248-298C>A ENSP00000455007.1:n.248-298C>A
NM_003321.4:c.375C>A NP_003312.3:p.Tyr125Ter
XM_011545928.1:c.375C>A XP_011544230.1:p.Tyr125Ter
NM_001365360.1:c.375C>A NP_001352289.1:p.Tyr125Ter
NM_003321.5:c.375C>A MANE Select NP_003312.3:p.Tyr125Ter
NM_001365360.2:c.375C>A NP_001352289.1:p.Tyr125Ter