Canonical Allele Identifier: CA341437808

Gene: WARS2 WARS2-AS1

Linked Data

• MyVariant Identifiers: chr1:g.119683230C>G (hg19) ; chr1:g.119140607C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140607C>G , CM000663.2:g.119140607C>G	GRCh38
NC_000001.10:g.119683230C>G , CM000663.1:g.119683230C>G	GRCh37
NC_000001.9:g.119484753C>G	NCBI36
NG_050658.1:g.5182G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.38G>C (WARS2) MANE Select	ENSP00000235521.4:p.Trp13Ser
ENST00000235521.4:c.38G>C (WARS2)	ENSP00000235521.4:p.Trp13Ser
ENST00000369426.9:c.38G>C (WARS2)	ENSP00000358434.5:p.Trp13Ser
ENST00000495746.5:n.48G>C (WARS2)
ENST00000497761.1:n.32G>C (WARS2)
NM_015836.3:c.38G>C (WARS2)	NP_056651.1:p.Trp13Ser
NM_201263.2:c.38G>C (WARS2)	NP_957715.1:p.Trp13Ser
NR_125974.1:n.212C>G (WARS2-AS1)
NR_125975.1:n.212C>G (WARS2-AS1)
NR_125976.1:n.212C>G (WARS2-AS1)
NR_125977.1:n.212C>G (WARS2-AS1)
XM_006710283.1:c.-532G>C (WARS2)	XP_006710346.1:n.-532G>C
XM_011540493.1:c.-404G>C (WARS2)	XP_011538795.1:n.-404G>C
XM_011540494.1:c.-117G>C (WARS2)	XP_011538796.1:n.-117G>C
XM_011540495.1:c.38G>C (WARS2)	XP_011538797.1:p.Trp13Ser
XM_011540494.2:c.-117G>C (WARS2)	XP_011538796.1:n.-117G>C
XM_011540495.2:c.38G>C (WARS2)	XP_011538797.1:p.Trp13Ser
XM_017000038.1:c.38G>C (WARS2)	XP_016855527.1:p.Trp13Ser
XM_017000039.1:c.-308G>C (WARS2)	XP_016855528.1:n.-308G>C
XM_017000040.1:c.38G>C (WARS2)	XP_016855529.1:p.Trp13Ser
XM_017000041.2:c.-532G>C (WARS2)	XP_016855530.1:n.-532G>C
XM_017000042.1:c.38G>C (WARS2)	XP_016855531.1:p.Trp13Ser
XM_024449826.1:c.-404G>C (WARS2)	XP_024305594.1:n.-404G>C
XM_024449860.1:c.-532G>C (WARS2)	XP_024305628.1:n.-532G>C
XM_024449871.1:c.-436G>C (WARS2)	XP_024305639.1:n.-436G>C
NM_001378226.1:c.-117G>C (WARS2)	NP_001365155.1:n.-117G>C
NM_001378227.1:c.-308G>C (WARS2)	NP_001365156.1:n.-308G>C
NM_001378228.1:c.38G>C (WARS2)	NP_001365157.1:p.Trp13Ser
NM_001378229.1:c.38G>C (WARS2)	NP_001365158.1:p.Trp13Ser
NM_001378230.1:c.-436G>C (WARS2)	NP_001365159.1:n.-436G>C
NM_001378231.1:c.38G>C (WARS2)	NP_001365160.1:p.Trp13Ser
NM_015836.4:c.38G>C (WARS2) MANE Select	NP_056651.1:p.Trp13Ser