Canonical Allele Identifier: CA1077117

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150504612C>G , CM000663.2:g.150504612C>G	GRCh38
NC_000001.10:g.150477088C>G , CM000663.1:g.150477088C>G	GRCh37
NC_000001.9:g.148743712C>G	NCBI36
NG_012062.1:g.1602C>G
NG_034226.1:g.22249C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025150.5:c.1719-20C>G MANE Select	NP_079426.2:n.1719-20C>G
ENST00000369064.8:c.1719-20C>G MANE Select	ENSP00000358060.3:n.1719-20C>G
NM_001271895.1:c.1473-20C>G	NP_001258824.1:n.1473-20C>G
NM_001271895.2:c.1473-20C>G	NP_001258824.1:n.1473-20C>G
NM_001271896.1:c.1329-20C>G	NP_001258825.1:n.1329-20C>G
NM_001271896.2:c.1329-20C>G	NP_001258825.1:n.1329-20C>G
NM_025150.4:c.1719-20C>G	NP_079426.2:n.1719-20C>G
NR_073513.1:n.1205-20C>G
NR_073513.2:n.1150-20C>G
NR_073514.1:n.1681-20C>G
NR_073514.2:n.1626-20C>G
ENST00000369051.7:c.*710-20C>G	ENSP00000358047.3:n.*710-20C>G
ENST00000369054.6:c.1329-20C>G	ENSP00000358050.2:n.1329-20C>G
ENST00000369064.7:c.1719-20C>G	ENSP00000358060.3:n.1719-20C>G
ENST00000438568.6:c.894-20C>G	ENSP00000415002.3:n.894-20C>G
ENST00000467982.6:c.1298-20C>G	ENSP00000475551.1:n.1298-20C>G
ENST00000483046.1:n.103+177C>G
ENST00000606933.5:c.1473-20C>G	ENSP00000475847.1:n.1473-20C>G
XM_006711555.1:c.1718+177C>G	XP_006711618.1:n.1718+177C>G
XM_006711555.2:c.1718+177C>G	XP_006711618.1:n.1718+177C>G
XM_006711556.1:c.1572-20C>G	XP_006711619.1:n.1572-20C>G
XM_011510009.1:c.1620-20C>G	XP_011508311.1:n.1620-20C>G
XM_017002394.2:c.1571+177C>G	XP_016857883.1:n.1571+177C>G
XM_017002395.2:c.1472+177C>G	XP_016857884.1:n.1472+177C>G