Canonical Allele Identifier: CA339681935

Gene: YARS1

Linked Data

• MyVariant Identifiers: chr1:g.33245875G>C (hg19) ; chr1:g.32780274G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780274G>C , CM000663.2:g.32780274G>C	GRCh38
NC_000001.10:g.33245875G>C , CM000663.1:g.33245875G>C	GRCh37
NC_000001.9:g.33018462G>C	NCBI36
NG_008408.1:g.42759C>G , LRG_273:g.42759C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.998C>G	ENSP00000502019.1:p.Pro333Arg
ENST00000373477.9:c.1145C>G MANE Select	ENSP00000362576.4:p.Pro382Arg
ENST00000674629.1:c.*693C>G	ENSP00000502470.1:n.*693C>G
ENST00000674654.1:c.*1105C>G	ENSP00000501729.1:n.*1105C>G
ENST00000675785.1:c.998C>G	ENSP00000502019.1:p.Pro333Arg
ENST00000676297.1:c.*1319C>G	ENSP00000501596.1:n.*1319C>G
ENST00000373477.8:c.1145C>G	ENSP00000362576.4:p.Pro382Arg
ENST00000469100.5:n.1061C>G
ENST00000478828.1:n.612C>G
ENST00000487404.5:n.1455C>G
ENST00000490826.1:n.438C>G
ENST00000616261.1:c.1144C>G	ENSP00000484192.1:p.Gln382Glu
NM_003680.3:c.1145C>G , LRG_273t1:c.1145C>G	NP_003671.1:p.Pro382Arg
XM_011542347.1:c.515C>G	XP_011540649.1:p.Pro172Arg
XM_011542348.1:c.515C>G	XP_011540650.1:p.Pro172Arg
XM_011542347.2:c.515C>G	XP_011540649.1:p.Pro172Arg
XM_017002651.2:c.515C>G	XP_016858140.1:p.Pro172Arg
NM_003680.4:c.1145C>G MANE Select	NP_003671.1:p.Pro382Arg