Canonical Allele Identifier: CA341437858

Gene: WARS2 WARS2-AS1

Linked Data

• gnomAD v4: 1-119140632-A-T
• MyVariant Identifiers: chr1:g.119683255A>T (hg19) ; chr1:g.119140632A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140632A>T , CM000663.2:g.119140632A>T	GRCh38
NC_000001.10:g.119683255A>T , CM000663.1:g.119683255A>T	GRCh37
NC_000001.9:g.119484778A>T	NCBI36
NG_050658.1:g.5157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.13T>A (WARS2) MANE Select	ENSP00000235521.4:p.Ser5Thr
ENST00000235521.4:c.13T>A (WARS2)	ENSP00000235521.4:p.Ser5Thr
ENST00000369426.9:c.13T>A (WARS2)	ENSP00000358434.5:p.Ser5Thr
ENST00000495746.5:n.23T>A (WARS2)
ENST00000497761.1:n.7T>A (WARS2)
NM_015836.3:c.13T>A (WARS2)	NP_056651.1:p.Ser5Thr
NM_201263.2:c.13T>A (WARS2)	NP_957715.1:p.Ser5Thr
NR_125974.1:n.237A>T (WARS2-AS1)
NR_125975.1:n.237A>T (WARS2-AS1)
NR_125976.1:n.237A>T (WARS2-AS1)
NR_125977.1:n.237A>T (WARS2-AS1)
XM_006710283.1:c.-557T>A (WARS2)	XP_006710346.1:n.-557T>A
XM_011540493.1:c.-429T>A (WARS2)	XP_011538795.1:n.-429T>A
XM_011540494.1:c.-142T>A (WARS2)	XP_011538796.1:n.-142T>A
XM_011540495.1:c.13T>A (WARS2)	XP_011538797.1:p.Ser5Thr
XM_011540494.2:c.-142T>A (WARS2)	XP_011538796.1:n.-142T>A
XM_011540495.2:c.13T>A (WARS2)	XP_011538797.1:p.Ser5Thr
XM_017000038.1:c.13T>A (WARS2)	XP_016855527.1:p.Ser5Thr
XM_017000039.1:c.-333T>A (WARS2)	XP_016855528.1:n.-333T>A
XM_017000040.1:c.13T>A (WARS2)	XP_016855529.1:p.Ser5Thr
XM_017000041.2:c.-557T>A (WARS2)	XP_016855530.1:n.-557T>A
XM_017000042.1:c.13T>A (WARS2)	XP_016855531.1:p.Ser5Thr
XM_024449826.1:c.-429T>A (WARS2)	XP_024305594.1:n.-429T>A
XM_024449860.1:c.-557T>A (WARS2)	XP_024305628.1:n.-557T>A
XM_024449871.1:c.-461T>A (WARS2)	XP_024305639.1:n.-461T>A
NM_001378226.1:c.-142T>A (WARS2)	NP_001365155.1:n.-142T>A
NM_001378227.1:c.-333T>A (WARS2)	NP_001365156.1:n.-333T>A
NM_001378228.1:c.13T>A (WARS2)	NP_001365157.1:p.Ser5Thr
NM_001378229.1:c.13T>A (WARS2)	NP_001365158.1:p.Ser5Thr
NM_001378230.1:c.-461T>A (WARS2)	NP_001365159.1:n.-461T>A
NM_001378231.1:c.13T>A (WARS2)	NP_001365160.1:p.Ser5Thr
NM_015836.4:c.13T>A (WARS2) MANE Select	NP_056651.1:p.Ser5Thr