Canonical Allele Identifier: CA1077164

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150504774G>A , CM000663.2:g.150504774G>A	GRCh38
NC_000001.10:g.150477250G>A , CM000663.1:g.150477250G>A	GRCh37
NC_000001.9:g.148743874G>A	NCBI36
NG_012062.1:g.1764G>A
NG_034226.1:g.22411G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025150.5:c.1820+41G>A MANE Select	NP_079426.2:n.1820+41G>A
ENST00000369064.8:c.1820+41G>A MANE Select	ENSP00000358060.3:n.1820+41G>A
NM_001271895.1:c.1574+41G>A	NP_001258824.1:n.1574+41G>A
NM_001271895.2:c.1574+41G>A	NP_001258824.1:n.1574+41G>A
NM_001271896.1:c.1430+41G>A	NP_001258825.1:n.1430+41G>A
NM_001271896.2:c.1430+41G>A	NP_001258825.1:n.1430+41G>A
NM_025150.4:c.1820+41G>A	NP_079426.2:n.1820+41G>A
NR_073513.1:n.1306+41G>A
NR_073513.2:n.1251+41G>A
NR_073514.1:n.1782+41G>A
NR_073514.2:n.1727+41G>A
ENST00000369051.7:c.*811+41G>A	ENSP00000358047.3:n.*811+41G>A
ENST00000369054.6:c.1430+41G>A	ENSP00000358050.2:n.1430+41G>A
ENST00000369064.7:c.1820+41G>A	ENSP00000358060.3:n.1820+41G>A
ENST00000438568.6:c.995+41G>A	ENSP00000415002.3:n.995+41G>A
ENST00000467982.6:c.1399+41G>A	ENSP00000475551.1:n.1399+41G>A
ENST00000483046.1:n.104-132G>A
ENST00000606933.5:c.1574+41G>A	ENSP00000475847.1:n.1574+41G>A
XM_006711555.1:c.1719-132G>A	XP_006711618.1:n.1719-132G>A
XM_006711555.2:c.1719-132G>A	XP_006711618.1:n.1719-132G>A
XM_006711556.1:c.1673+41G>A	XP_006711619.1:n.1673+41G>A
XM_011510009.1:c.1721+41G>A	XP_011508311.1:n.1721+41G>A
XM_017002394.2:c.1572-132G>A	XP_016857883.1:n.1572-132G>A
XM_017002395.2:c.1473-132G>A	XP_016857884.1:n.1473-132G>A