Canonical Allele Identifier: CA1077000

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150498681T>A , CM000663.2:g.150498681T>A	GRCh38
NC_000001.10:g.150471157T>A , CM000663.1:g.150471157T>A	GRCh37
NC_000001.9:g.148737781T>A	NCBI36
NG_034226.1:g.16318T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025150.5:c.1401+17T>A MANE Select	NP_079426.2:n.1401+17T>A
ENST00000369064.8:c.1401+17T>A MANE Select	ENSP00000358060.3:n.1401+17T>A
NM_001271895.1:c.1155+17T>A	NP_001258824.1:n.1155+17T>A
NM_001271895.2:c.1155+17T>A	NP_001258824.1:n.1155+17T>A
NM_001271896.1:c.1011+17T>A	NP_001258825.1:n.1011+17T>A
NM_001271896.2:c.1011+17T>A	NP_001258825.1:n.1011+17T>A
NM_025150.4:c.1401+17T>A	NP_079426.2:n.1401+17T>A
NR_073513.1:n.887+17T>A
NR_073513.2:n.832+17T>A
NR_073514.1:n.1363+17T>A
NR_073514.2:n.1308+17T>A
ENST00000369051.7:c.*392+17T>A	ENSP00000358047.3:n.*392+17T>A
ENST00000369054.6:c.1011+17T>A	ENSP00000358050.2:n.1011+17T>A
ENST00000369064.7:c.1401+17T>A	ENSP00000358060.3:n.1401+17T>A
ENST00000438568.6:c.576+17T>A	ENSP00000415002.3:n.576+17T>A
ENST00000463555.1:n.534+17T>A
ENST00000467982.6:c.980+17T>A	ENSP00000475551.1:n.980+17T>A
ENST00000480070.5:n.514+17T>A
ENST00000606933.5:c.1155+17T>A	ENSP00000475847.1:n.1155+17T>A
XM_006711555.1:c.1401+17T>A	XP_006711618.1:n.1401+17T>A
XM_006711555.2:c.1401+17T>A	XP_006711618.1:n.1401+17T>A
XM_006711556.1:c.1254+17T>A	XP_006711619.1:n.1254+17T>A
XM_011510009.1:c.1302+17T>A	XP_011508311.1:n.1302+17T>A
XM_017002394.2:c.1254+17T>A	XP_016857883.1:n.1254+17T>A
XM_017002395.2:c.1155+17T>A	XP_016857884.1:n.1155+17T>A