Canonical Allele Identifier: CA417066586

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32797775G>A , CM000663.2:g.32797775G>A	GRCh38
NC_000001.10:g.33263376G>A , CM000663.1:g.33263376G>A	GRCh37
NC_000001.9:g.33035963G>A	NCBI36
NG_008408.1:g.25258C>T , LRG_273:g.25258C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003680.4:c.579C>T MANE Select	NP_003671.1:p.Thr193=
ENST00000373477.9:c.579C>T MANE Select	ENSP00000362576.4:p.Thr193=
NM_003680.3:c.579C>T , LRG_273t1:c.579C>T	NP_003671.1:p.Thr193=
ENST00000373477.8:c.579C>T	ENSP00000362576.4:p.Thr193=
ENST00000466052.1:n.440C>T
ENST00000470377.1:n.168C>T
ENST00000481895.5:n.652C>T
ENST00000481895.6:c.579C>T	ENSP00000502016.1:p.Thr193=
ENST00000616261.1:c.579C>T	ENSP00000484192.1:p.Thr193=
ENST00000616261.2:c.579C>T	ENSP00000484192.2:p.Thr193=
ENST00000674629.1:c.*127C>T	ENSP00000502470.1:n.*127C>T
ENST00000674654.1:c.*47C>T	ENSP00000501729.1:n.*47C>T
ENST00000675785.1:c.432C>T	ENSP00000502019.1:p.Thr144=
ENST00000675785.2:c.432C>T	ENSP00000502019.1:p.Thr144=
ENST00000676297.1:c.*261C>T	ENSP00000501596.1:n.*261C>T
XM_011542347.1:c.-52C>T	XP_011540649.1:n.-52C>T
XM_011542347.2:c.-52C>T	XP_011540649.1:n.-52C>T
XM_011542348.1:c.-99C>T	XP_011540650.1:n.-99C>T
XM_017002651.2:c.-99C>T	XP_016858140.1:n.-99C>T