Canonical Allele Identifier: CA1192128169

Gene: WARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033137G= , CM000663.2:g.119033137G=	GRCh38
NC_000001.10:g.119575760G= , CM000663.1:g.119575760G=	GRCh37
NC_000001.9:g.119377283G=	NCBI36
NG_050658.1:g.112652C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.857C= MANE Select	ENSP00000235521.4:p.Ser286=
ENST00000235521.4:c.857C=	ENSP00000235521.4:p.Ser286=
ENST00000369426.9:c.*223C=	ENSP00000358434.5:n.*223C=
NM_015836.3:c.857C=	NP_056651.1:p.Ser286=
NM_201263.2:c.*223C=	NP_957715.1:n.*223C=
XM_005270350.2:c.803C=	XP_005270407.1:p.Ser268=
XM_006710283.1:c.575C=	XP_006710346.1:p.Ser192=
XM_011540493.1:c.788C=	XP_011538795.1:p.Ser263=
XM_011540494.1:c.788C=	XP_011538796.1:p.Ser263=
XM_011540495.1:c.599C=	XP_011538797.1:p.Ser200=
XM_005270350.3:c.803C=	XP_005270407.1:p.Ser268=
XM_011540494.2:c.788C=	XP_011538796.1:p.Ser263=
XM_011540495.2:c.599C=	XP_011538797.1:p.Ser200=
XM_017000038.1:c.800C=	XP_016855527.1:p.Ser267=
XM_017000039.1:c.788C=	XP_016855528.1:p.Ser263=
XM_017000040.1:c.686C=	XP_016855529.1:p.Ser229=
XM_017000041.2:c.518C=	XP_016855530.1:p.Ser173=
XM_017000042.1:c.*192C=	XP_016855531.1:n.*192C=
XM_024449826.1:c.788C=	XP_024305594.1:p.Ser263=
XM_024449860.1:c.575C=	XP_024305628.1:p.Ser192=
XM_024449871.1:c.575C=	XP_024305639.1:p.Ser192=
NM_001378226.1:c.788C=	NP_001365155.1:p.Ser263=
NM_001378227.1:c.788C=	NP_001365156.1:p.Ser263=
NM_001378228.1:c.686C=	NP_001365157.1:p.Ser229=
NM_001378229.1:c.599C=	NP_001365158.1:p.Ser200=
NM_001378230.1:c.575C=	NP_001365159.1:p.Ser192=
NM_001378231.1:c.*192C=	NP_001365160.1:n.*192C=
NM_015836.4:c.857C= MANE Select	NP_056651.1:p.Ser286=