Canonical Allele Identifier: CA339681526

Gene: YARS1

Linked Data

• MyVariant Identifiers: chr1:g.33245772C>G (hg19) ; chr1:g.32780171C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780171C>G , CM000663.2:g.32780171C>G	GRCh38
NC_000001.10:g.33245772C>G , CM000663.1:g.33245772C>G	GRCh37
NC_000001.9:g.33018359C>G	NCBI36
NG_008408.1:g.42862G>C , LRG_273:g.42862G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1101G>C	ENSP00000502019.1:p.Gln367His
ENST00000373477.9:c.1248G>C MANE Select	ENSP00000362576.4:p.Gln416His
ENST00000674629.1:c.*796G>C	ENSP00000502470.1:n.*796G>C
ENST00000674654.1:c.*1208G>C	ENSP00000501729.1:n.*1208G>C
ENST00000675785.1:c.1101G>C	ENSP00000502019.1:p.Gln367His
ENST00000676297.1:c.*1422G>C	ENSP00000501596.1:n.*1422G>C
ENST00000373477.8:c.1248G>C	ENSP00000362576.4:p.Gln416His
ENST00000469100.5:n.1164G>C
ENST00000478828.1:n.715G>C
ENST00000487404.5:n.1558G>C
ENST00000490826.1:n.541G>C
NM_003680.3:c.1248G>C , LRG_273t1:c.1248G>C	NP_003671.1:p.Gln416His
XM_011542347.1:c.618G>C	XP_011540649.1:p.Gln206His
XM_011542348.1:c.618G>C	XP_011540650.1:p.Gln206His
XM_011542347.2:c.618G>C	XP_011540649.1:p.Gln206His
XM_017002651.2:c.618G>C	XP_016858140.1:p.Gln206His
NM_003680.4:c.1248G>C MANE Select	NP_003671.1:p.Gln416His