Canonical Allele Identifier: CA339683249

Gene: YARS1

Linked Data

• MyVariant Identifiers: chr1:g.33248007T>C (hg19) ; chr1:g.32782406T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32782406T>C , CM000663.2:g.32782406T>C	GRCh38
NC_000001.10:g.33248007T>C , CM000663.1:g.33248007T>C	GRCh37
NC_000001.9:g.33020594T>C	NCBI36
NG_008408.1:g.40627A>G , LRG_273:g.40627A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000675785.2:c.893A>G	ENSP00000502019.1:p.Gln298Arg
ENST00000373477.9:c.1040A>G MANE Select	ENSP00000362576.4:p.Gln347Arg
ENST00000674629.1:c.*588A>G	ENSP00000502470.1:n.*588A>G
ENST00000674654.1:c.*1000A>G	ENSP00000501729.1:n.*1000A>G
ENST00000675785.1:c.893A>G	ENSP00000502019.1:p.Gln298Arg
ENST00000676297.1:c.*1214A>G	ENSP00000501596.1:n.*1214A>G
ENST00000373477.8:c.1040A>G	ENSP00000362576.4:p.Gln347Arg
ENST00000478828.1:n.507A>G
ENST00000487404.5:n.1350A>G
ENST00000616261.1:c.1040A>G	ENSP00000484192.1:p.Gln347Arg
NM_003680.3:c.1040A>G , LRG_273t1:c.1040A>G	NP_003671.1:p.Gln347Arg
XM_011542347.1:c.410A>G	XP_011540649.1:p.Gln137Arg
XM_011542348.1:c.410A>G	XP_011540650.1:p.Gln137Arg
XM_011542347.2:c.410A>G	XP_011540649.1:p.Gln137Arg
XM_017002651.2:c.410A>G	XP_016858140.1:p.Gln137Arg
NM_003680.4:c.1040A>G MANE Select	NP_003671.1:p.Gln347Arg