Canonical Allele Identifier: CA420192694

Gene: WARS2

Linked Data

• gnomAD v4: 1-119033208-G-A
• MyVariant Identifiers: chr1:g.119575831G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033208G>A , CM000663.2:g.119033208G>A	GRCh38
NC_000001.10:g.119575831G>A , CM000663.1:g.119575831G>A	GRCh37
NC_000001.9:g.119377354G>A	NCBI36
NG_050658.1:g.112581C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.786C>T MANE Select	ENSP00000235521.4:p.Val262=
ENST00000235521.4:c.786C>T	ENSP00000235521.4:p.Val262=
ENST00000369426.9:c.*152C>T	ENSP00000358434.5:n.*152C>T
NM_015836.3:c.786C>T	NP_056651.1:p.Val262=
NM_201263.2:c.*152C>T	NP_957715.1:n.*152C>T
XM_005270350.2:c.732C>T	XP_005270407.1:p.Val244=
XM_006710283.1:c.504C>T	XP_006710346.1:p.Val168=
XM_011540493.1:c.717C>T	XP_011538795.1:p.Val239=
XM_011540494.1:c.717C>T	XP_011538796.1:p.Val239=
XM_011540495.1:c.528C>T	XP_011538797.1:p.Val176=
XM_005270350.3:c.732C>T	XP_005270407.1:p.Val244=
XM_011540494.2:c.717C>T	XP_011538796.1:p.Val239=
XM_011540495.2:c.528C>T	XP_011538797.1:p.Val176=
XM_017000038.1:c.729C>T	XP_016855527.1:p.Val243=
XM_017000039.1:c.717C>T	XP_016855528.1:p.Val239=
XM_017000040.1:c.615C>T	XP_016855529.1:p.Val205=
XM_017000041.2:c.447C>T	XP_016855530.1:p.Val149=
XM_017000042.1:c.*121C>T	XP_016855531.1:n.*121C>T
XM_024449826.1:c.717C>T	XP_024305594.1:p.Val239=
XM_024449860.1:c.504C>T	XP_024305628.1:p.Val168=
XM_024449871.1:c.504C>T	XP_024305639.1:p.Val168=
NM_001378226.1:c.717C>T	NP_001365155.1:p.Val239=
NM_001378227.1:c.717C>T	NP_001365156.1:p.Val239=
NM_001378228.1:c.615C>T	NP_001365157.1:p.Val205=
NM_001378229.1:c.528C>T	NP_001365158.1:p.Val176=
NM_001378230.1:c.504C>T	NP_001365159.1:p.Val168=
NM_001378231.1:c.*121C>T	NP_001365160.1:n.*121C>T
NM_015836.4:c.786C>T MANE Select	NP_056651.1:p.Val262=