Canonical Allele Identifier: CA745029

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32782434T>C , CM000663.2:g.32782434T>C	GRCh38
NC_000001.10:g.33248035T>C , CM000663.1:g.33248035T>C	GRCh37
NC_000001.9:g.33020622T>C	NCBI36
NG_008408.1:g.40599A>G , LRG_273:g.40599A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003680.4:c.1012A>G MANE Select	NP_003671.1:p.Ser338Gly
ENST00000373477.9:c.1012A>G MANE Select	ENSP00000362576.4:p.Ser338Gly
NM_003680.3:c.1012A>G , LRG_273t1:c.1012A>G	NP_003671.1:p.Ser338Gly
ENST00000373477.8:c.1012A>G	ENSP00000362576.4:p.Ser338Gly
ENST00000478828.1:n.479A>G
ENST00000487404.5:n.1322A>G
ENST00000616261.1:c.1012A>G	ENSP00000484192.1:p.Ser338Gly
ENST00000674629.1:c.*560A>G	ENSP00000502470.1:n.*560A>G
ENST00000674654.1:c.*972A>G	ENSP00000501729.1:n.*972A>G
ENST00000675785.1:c.865A>G	ENSP00000502019.1:p.Ser289Gly
ENST00000675785.2:c.865A>G	ENSP00000502019.1:p.Ser289Gly
ENST00000676297.1:c.*1186A>G	ENSP00000501596.1:n.*1186A>G
XM_011542347.1:c.382A>G	XP_011540649.1:p.Ser128Gly
XM_011542347.2:c.382A>G	XP_011540649.1:p.Ser128Gly
XM_011542348.1:c.382A>G	XP_011540650.1:p.Ser128Gly
XM_017002651.2:c.382A>G	XP_016858140.1:p.Ser128Gly