Canonical Allele Identifier: CA395417606

Gene: TUFM

Linked Data

• MyVariant Identifiers: chr16:g.28856318T>C (hg19) ; chr16:g.28844997T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28844997T>C , CM000678.2:g.28844997T>C	GRCh38
NC_000016.9:g.28856318T>C , CM000678.1:g.28856318T>C	GRCh37
NC_000016.8:g.28763819T>C	NCBI36
NG_008964.1:g.6412A>G
NG_029706.2:g.3398T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313511.8:c.473A>G MANE Select	ENSP00000322439.3:p.Asp158Gly
ENST00000313511.7:c.473A>G	ENSP00000322439.3:p.Asp158Gly
ENST00000561644.1:n.11A>G
ENST00000565012.1:c.306A>G	ENSP00000455007.1:p.Ter102Trp
NM_003321.4:c.473A>G	NP_003312.3:p.Asp158Gly
XM_011545928.1:c.473A>G	XP_011544230.1:p.Asp158Gly
NM_001365360.1:c.473A>G	NP_001352289.1:p.Asp158Gly
NM_003321.5:c.473A>G MANE Select	NP_003312.3:p.Asp158Gly
NM_001365360.2:c.473A>G	NP_001352289.1:p.Asp158Gly