Canonical Allele Identifier: CA339681606

Gene: YARS1

Linked Data

• gnomAD v4: 1-32780194-A-G
• MyVariant Identifiers: chr1:g.33245795A>G (hg19) ; chr1:g.32780194A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780194A>G , CM000663.2:g.32780194A>G	GRCh38
NC_000001.10:g.33245795A>G , CM000663.1:g.33245795A>G	GRCh37
NC_000001.9:g.33018382A>G	NCBI36
NG_008408.1:g.42839T>C , LRG_273:g.42839T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1078T>C	ENSP00000502019.1:p.Phe360Leu
ENST00000373477.9:c.1225T>C MANE Select	ENSP00000362576.4:p.Phe409Leu
ENST00000674629.1:c.*773T>C	ENSP00000502470.1:n.*773T>C
ENST00000674654.1:c.*1185T>C	ENSP00000501729.1:n.*1185T>C
ENST00000675785.1:c.1078T>C	ENSP00000502019.1:p.Phe360Leu
ENST00000676297.1:c.*1399T>C	ENSP00000501596.1:n.*1399T>C
ENST00000373477.8:c.1225T>C	ENSP00000362576.4:p.Phe409Leu
ENST00000469100.5:n.1141T>C
ENST00000478828.1:n.692T>C
ENST00000487404.5:n.1535T>C
ENST00000490826.1:n.518T>C
NM_003680.3:c.1225T>C , LRG_273t1:c.1225T>C	NP_003671.1:p.Phe409Leu
XM_011542347.1:c.595T>C	XP_011540649.1:p.Phe199Leu
XM_011542348.1:c.595T>C	XP_011540650.1:p.Phe199Leu
XM_011542347.2:c.595T>C	XP_011540649.1:p.Phe199Leu
XM_017002651.2:c.595T>C	XP_016858140.1:p.Phe199Leu
NM_003680.4:c.1225T>C MANE Select	NP_003671.1:p.Phe409Leu