Canonical Allele Identifier: CA30376561

Gene: WARS2

Linked Data

• dbSNP Id: rs148415181
• MyVariant Identifiers: chr1:g.119575782_119575783insGC (hg19) ; chr1:g.119033159_119033160insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033159_119033160insGC , CM000663.2:g.119033159_119033160insGC	GRCh38
NC_000001.10:g.119575782_119575783insGC , CM000663.1:g.119575782_119575783insGC	GRCh37
NC_000001.9:g.119377305_119377306insGC	NCBI36
NG_050658.1:g.112629_112630insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.834_835insGC MANE Select	ENSP00000235521.4:p.His279AlafsTer5
ENST00000235521.4:c.834_835insGC	ENSP00000235521.4:p.His279AlafsTer5
ENST00000369426.9:c.*200_*201insGC	ENSP00000358434.5:n.*200_*201insGC
NM_015836.3:c.834_835insGC	NP_056651.1:p.His279AlafsTer5
NM_201263.2:c.*200_*201insGC	NP_957715.1:n.*200_*201insGC
XM_005270350.2:c.780_781insGC	XP_005270407.1:p.His261AlafsTer5
XM_006710283.1:c.552_553insGC	XP_006710346.1:p.His185AlafsTer5
XM_011540493.1:c.765_766insGC	XP_011538795.1:p.His256AlafsTer5
XM_011540494.1:c.765_766insGC	XP_011538796.1:p.His256AlafsTer5
XM_011540495.1:c.576_577insGC	XP_011538797.1:p.His193AlafsTer5
XM_005270350.3:c.780_781insGC	XP_005270407.1:p.His261AlafsTer5
XM_011540494.2:c.765_766insGC	XP_011538796.1:p.His256AlafsTer5
XM_011540495.2:c.576_577insGC	XP_011538797.1:p.His193AlafsTer5
XM_017000038.1:c.777_778insGC	XP_016855527.1:p.His260AlafsTer5
XM_017000039.1:c.765_766insGC	XP_016855528.1:p.His256AlafsTer5
XM_017000040.1:c.663_664insGC	XP_016855529.1:p.His222AlafsTer5
XM_017000041.2:c.495_496insGC	XP_016855530.1:p.His166AlafsTer5
XM_017000042.1:c.*169_*170insGC	XP_016855531.1:n.*169_*170insGC
XM_024449826.1:c.765_766insGC	XP_024305594.1:p.His256AlafsTer5
XM_024449860.1:c.552_553insGC	XP_024305628.1:p.His185AlafsTer5
XM_024449871.1:c.552_553insGC	XP_024305639.1:p.His185AlafsTer5
NM_001378226.1:c.765_766insGC	NP_001365155.1:p.His256AlafsTer5
NM_001378227.1:c.765_766insGC	NP_001365156.1:p.His256AlafsTer5
NM_001378228.1:c.663_664insGC	NP_001365157.1:p.His222AlafsTer5
NM_001378229.1:c.576_577insGC	NP_001365158.1:p.His193AlafsTer5
NM_001378230.1:c.552_553insGC	NP_001365159.1:p.His185AlafsTer5
NM_001378231.1:c.*169_*170insGC	NP_001365160.1:n.*169_*170insGC
NM_015836.4:c.834_835insGC MANE Select	NP_056651.1:p.His279AlafsTer5