Canonical Allele Identifier: CA15086726

Gene: TARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150491050T>C , CM000663.2:g.150491050T>C	GRCh38
NC_000001.10:g.150463526T>C , CM000663.1:g.150463526T>C	GRCh37
NC_000001.9:g.148730150T>C	NCBI36
NG_034226.1:g.8687T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025150.5:c.512+325T>C MANE Select	NP_079426.2:n.512+325T>C
ENST00000369064.8:c.512+325T>C MANE Select	ENSP00000358060.3:n.512+325T>C
NM_001271895.1:c.512+325T>C	NP_001258824.1:n.512+325T>C
NM_001271895.2:c.512+325T>C	NP_001258824.1:n.512+325T>C
NM_001271896.1:c.512+325T>C	NP_001258825.1:n.512+325T>C
NM_001271896.2:c.512+325T>C	NP_001258825.1:n.512+325T>C
NM_025150.4:c.512+325T>C	NP_079426.2:n.512+325T>C
NR_073513.1:n.427+325T>C
NR_073513.2:n.372+325T>C
NR_073514.1:n.475-344T>C
NR_073514.2:n.420-344T>C
ENST00000369051.7:c.340+325T>C	ENSP00000358047.3:n.340+325T>C
ENST00000369054.6:c.512+325T>C	ENSP00000358050.2:n.512+325T>C
ENST00000369064.7:c.512+325T>C	ENSP00000358060.3:n.512+325T>C
ENST00000438568.6:c.116+325T>C	ENSP00000415002.3:n.116+325T>C
ENST00000466989.1:n.189-344T>C
ENST00000467982.6:c.310-344T>C	ENSP00000475551.1:n.310-344T>C
ENST00000606933.5:c.512+325T>C	ENSP00000475847.1:n.512+325T>C
XM_006711555.1:c.512+325T>C	XP_006711618.1:n.512+325T>C
XM_006711555.2:c.512+325T>C	XP_006711618.1:n.512+325T>C
XM_006711556.1:c.512+325T>C	XP_006711619.1:n.512+325T>C
XM_011510009.1:c.512+325T>C	XP_011508311.1:n.512+325T>C
XM_017002394.2:c.512+325T>C	XP_016857883.1:n.512+325T>C
XM_017002395.2:c.512+325T>C	XP_016857884.1:n.512+325T>C