Canonical Allele Identifier: CA494484804

Gene: TUFM

Linked Data

• dbSNP Id: rs1316371660
• gnomAD v3: 16-28845023-G-T
• gnomAD v4: 16-28845023-G-T
• MyVariant Identifiers: chr16:g.28856344G>T (hg19) ; chr16:g.28845023G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28845023G>T , CM000678.2:g.28845023G>T	GRCh38
NC_000016.9:g.28856344G>T , CM000678.1:g.28856344G>T	GRCh37
NC_000016.8:g.28763845G>T	NCBI36
NG_008964.1:g.6386C>A
NG_029706.2:g.3424G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313511.8:c.447C>A MANE Select	ENSP00000322439.3:p.Gly149=
ENST00000313511.7:c.447C>A	ENSP00000322439.3:p.Gly149=
ENST00000565012.1:c.280C>A	ENSP00000455007.1:p.Leu94Met
NM_003321.4:c.447C>A	NP_003312.3:p.Gly149=
XM_011545928.1:c.447C>A	XP_011544230.1:p.Gly149=
NM_001365360.1:c.447C>A	NP_001352289.1:p.Gly149=
NM_003321.5:c.447C>A MANE Select	NP_003312.3:p.Gly149=
NM_001365360.2:c.447C>A	NP_001352289.1:p.Gly149=