Canonical Allele Identifier: CA2215863238
Gene: TUFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845029G= , CM000678.2:g.28845029G= GRCh38
NC_000016.9:g.28856350G= , CM000678.1:g.28856350G= GRCh37
NC_000016.8:g.28763851G= NCBI36
NG_008964.1:g.6380C=
NG_029706.2:g.3430G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.441C= MANE Select ENSP00000322439.3:p.Leu147=
ENST00000313511.7:c.441C= ENSP00000322439.3:p.Leu147=
ENST00000565012.1:c.274C= ENSP00000455007.1:p.Arg92=
NM_003321.4:c.441C= NP_003312.3:p.Leu147=
XM_011545928.1:c.441C= XP_011544230.1:p.Leu147=
NM_001365360.1:c.441C= NP_001352289.1:p.Leu147=
NM_003321.5:c.441C= MANE Select NP_003312.3:p.Leu147=
NM_001365360.2:c.441C= NP_001352289.1:p.Leu147=