Canonical Allele Identifier: CA2647372064

Gene: WARS2

Linked Data

• gnomAD v4: 1-119140338-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140338G>T , CM000663.2:g.119140338G>T	GRCh38
NC_000001.10:g.119682961G>T , CM000663.1:g.119682961G>T	GRCh37
NC_000001.9:g.119484484G>T	NCBI36
NG_050658.1:g.5451C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.90+217C>A MANE Select	ENSP00000235521.4:n.90+217C>A
ENST00000235521.4:c.90+217C>A	ENSP00000235521.4:n.90+217C>A
ENST00000369426.9:c.90+217C>A	ENSP00000358434.5:n.90+217C>A
ENST00000495746.5:n.100+217C>A
ENST00000497761.1:n.205C>A
NM_015836.3:c.90+217C>A	NP_056651.1:n.90+217C>A
NM_201263.2:c.90+217C>A	NP_957715.1:n.90+217C>A
XM_006710283.1:c.-263C>A	XP_006710346.1:n.-263C>A
XM_011540493.1:c.-135C>A	XP_011538795.1:n.-135C>A
XM_011540494.1:c.-65+217C>A	XP_011538796.1:n.-65+217C>A
XM_011540495.1:c.90+217C>A	XP_011538797.1:n.90+217C>A
XM_011540494.2:c.-65+217C>A	XP_011538796.1:n.-65+217C>A
XM_011540495.2:c.90+217C>A	XP_011538797.1:n.90+217C>A
XM_017000038.1:c.90+217C>A	XP_016855527.1:n.90+217C>A
XM_017000039.1:c.-135C>A	XP_016855528.1:n.-135C>A
XM_017000040.1:c.90+217C>A	XP_016855529.1:n.90+217C>A
XM_017000041.2:c.-263C>A	XP_016855530.1:n.-263C>A
XM_017000042.1:c.90+217C>A	XP_016855531.1:n.90+217C>A
XM_024449826.1:c.-135C>A	XP_024305594.1:n.-135C>A
XM_024449860.1:c.-263C>A	XP_024305628.1:n.-263C>A
XM_024449871.1:c.-263C>A	XP_024305639.1:n.-263C>A
NM_001378226.1:c.-65+217C>A	NP_001365155.1:n.-65+217C>A
NM_001378227.1:c.-135C>A	NP_001365156.1:n.-135C>A
NM_001378228.1:c.90+217C>A	NP_001365157.1:n.90+217C>A
NM_001378229.1:c.90+217C>A	NP_001365158.1:n.90+217C>A
NM_001378230.1:c.-263C>A	NP_001365159.1:n.-263C>A
NM_001378231.1:c.90+217C>A	NP_001365160.1:n.90+217C>A
NM_015836.4:c.90+217C>A MANE Select	NP_056651.1:n.90+217C>A