Canonical Allele Identifier: CA2574301836
Gene: YARS1 HGNC NCBI

Linked Data

gnomAD v4: 1-32780293-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780293C>A , CM000663.2:g.32780293C>A GRCh38
NC_000001.10:g.33245894C>A , CM000663.1:g.33245894C>A GRCh37
NC_000001.9:g.33018481C>A NCBI36
NG_008408.1:g.42740G>T , LRG_273:g.42740G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.994-15G>T ENSP00000502019.1:n.994-15G>T
ENST00000373477.9:c.1141-15G>T MANE Select ENSP00000362576.4:n.1141-15G>T
ENST00000674629.1:c.*689-15G>T ENSP00000502470.1:n.*689-15G>T
ENST00000674654.1:c.*1101-15G>T ENSP00000501729.1:n.*1101-15G>T
ENST00000675785.1:c.994-15G>T ENSP00000502019.1:n.994-15G>T
ENST00000676297.1:c.*1315-15G>T ENSP00000501596.1:n.*1315-15G>T
ENST00000373477.8:c.1141-15G>T ENSP00000362576.4:n.1141-15G>T
ENST00000469100.5:n.1057-15G>T
ENST00000478828.1:n.608-15G>T
ENST00000487404.5:n.1451-15G>T
ENST00000490826.1:n.419G>T
ENST00000616261.1:c.1140-15G>T ENSP00000484192.1:n.1140-15G>T
NM_003680.3:c.1141-15G>T , LRG_273t1:c.1141-15G>T NP_003671.1:n.1141-15G>T
XM_011542347.1:c.511-15G>T XP_011540649.1:n.511-15G>T
XM_011542348.1:c.511-15G>T XP_011540650.1:n.511-15G>T
XM_011542347.2:c.511-15G>T XP_011540649.1:n.511-15G>T
XM_017002651.2:c.511-15G>T XP_016858140.1:n.511-15G>T
NM_003680.4:c.1141-15G>T MANE Select NP_003671.1:n.1141-15G>T