Canonical Allele Identifier: CA395417963
Gene: TUFM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845319C>G , CM000678.2:g.28845319C>G GRCh38
NC_000016.9:g.28856640C>G , CM000678.1:g.28856640C>G GRCh37
NC_000016.8:g.28764141C>G NCBI36
NG_008964.1:g.6090G>C
NG_029706.2:g.3720C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313511.8:c.409G>C MANE Select ENSP00000322439.3:p.Val137Leu
ENST00000313511.7:c.409G>C ENSP00000322439.3:p.Val137Leu
ENST00000565012.1:c.248-264G>C ENSP00000455007.1:n.248-264G>C
NM_003321.4:c.409G>C NP_003312.3:p.Val137Leu
XM_011545928.1:c.409G>C XP_011544230.1:p.Val137Leu
NM_001365360.1:c.409G>C NP_001352289.1:p.Val137Leu
NM_003321.5:c.409G>C MANE Select NP_003312.3:p.Val137Leu
NM_001365360.2:c.409G>C NP_001352289.1:p.Val137Leu