Canonical Allele Identifier: CA1076963

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150498514C>T , CM000663.2:g.150498514C>T	GRCh38
NC_000001.10:g.150470990C>T , CM000663.1:g.150470990C>T	GRCh37
NC_000001.9:g.148737614C>T	NCBI36
NG_034226.1:g.16151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369064.8:c.1251C>T MANE Select	ENSP00000358060.3:p.Ala417=
ENST00000369051.7:c.*242C>T	ENSP00000358047.3:n.*242C>T
ENST00000369054.6:c.861C>T	ENSP00000358050.2:p.Ala287=
ENST00000369064.7:c.1251C>T	ENSP00000358060.3:p.Ala417=
ENST00000438568.6:c.426C>T	ENSP00000415002.3:p.Ala142=
ENST00000463555.1:n.384C>T
ENST00000467982.6:c.830C>T	ENSP00000475551.1:n.830C>T
ENST00000480070.5:n.364C>T
ENST00000606933.5:c.1005C>T	ENSP00000475847.1:p.Ala335=
NM_001271895.1:c.1005C>T	NP_001258824.1:p.Ala335=
NM_001271896.1:c.861C>T	NP_001258825.1:p.Ala287=
NM_025150.4:c.1251C>T	NP_079426.2:p.Ala417=
NR_073513.1:n.737C>T
NR_073514.1:n.1213C>T
XM_006711555.1:c.1251C>T	XP_006711618.1:p.Ala417=
XM_006711556.1:c.1104C>T	XP_006711619.1:p.Ala368=
XM_011510009.1:c.1152C>T	XP_011508311.1:p.Ala384=
XM_006711555.2:c.1251C>T	XP_006711618.1:p.Ala417=
XM_017002394.2:c.1104C>T	XP_016857883.1:p.Ala368=
XM_017002395.2:c.1005C>T	XP_016857884.1:p.Ala335=
NM_025150.5:c.1251C>T MANE Select	NP_079426.2:p.Ala417=
NM_001271895.2:c.1005C>T	NP_001258824.1:p.Ala335=
NM_001271896.2:c.861C>T	NP_001258825.1:p.Ala287=
NR_073513.2:n.682C>T
NR_073514.2:n.1158C>T