Canonical Allele Identifier: CA494484759

Gene: TUFM

Linked Data

• MyVariant Identifiers: chr16:g.28856281C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28844960C>G , CM000678.2:g.28844960C>G	GRCh38
NC_000016.9:g.28856281C>G , CM000678.1:g.28856281C>G	GRCh37
NC_000016.8:g.28763782C>G	NCBI36
NG_008964.1:g.6449G>C
NG_029706.2:g.3361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313511.8:c.510G>C MANE Select	ENSP00000322439.3:p.Leu170=
ENST00000313511.7:c.510G>C	ENSP00000322439.3:p.Leu170=
ENST00000561644.1:n.48G>C
ENST00000565012.1:c.*37G>C	ENSP00000455007.1:n.*37G>C
NM_003321.4:c.510G>C	NP_003312.3:p.Leu170=
XM_011545928.1:c.510G>C	XP_011544230.1:p.Leu170=
NM_001365360.1:c.510G>C	NP_001352289.1:p.Leu170=
NM_003321.5:c.510G>C MANE Select	NP_003312.3:p.Leu170=
NM_001365360.2:c.510G>C	NP_001352289.1:p.Leu170=