Canonical Allele Identifier: CA7985627

Gene: TUFM

Linked Data

• dbSNP Id: rs781744069
• ExAC: 16:28856309 A / G
• gnomAD v4: 16-28844988-A-G
• MyVariant Identifiers: chr16:g.28856309A>G (hg19) ; chr16:g.28844988A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28844988A>G , CM000678.2:g.28844988A>G	GRCh38
NC_000016.9:g.28856309A>G , CM000678.1:g.28856309A>G	GRCh37
NC_000016.8:g.28763810A>G	NCBI36
NG_008964.1:g.6421T>C
NG_029706.2:g.3389A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313511.8:c.482T>C MANE Select	ENSP00000322439.3:p.Met161Thr
ENST00000313511.7:c.482T>C	ENSP00000322439.3:p.Met161Thr
ENST00000561644.1:n.20T>C
ENST00000565012.1:c.*9T>C	ENSP00000455007.1:n.*9T>C
NM_003321.4:c.482T>C	NP_003312.3:p.Met161Thr
XM_011545928.1:c.482T>C	XP_011544230.1:p.Met161Thr
NM_001365360.1:c.482T>C	NP_001352289.1:p.Met161Thr
NM_003321.5:c.482T>C MANE Select	NP_003312.3:p.Met161Thr
NM_001365360.2:c.482T>C	NP_001352289.1:p.Met161Thr