Canonical Allele Identifier: CA2574301855
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780377G>C , CM000663.2:g.32780377G>C GRCh38
NC_000001.10:g.33245978G>C , CM000663.1:g.33245978G>C GRCh37
NC_000001.9:g.33018565G>C NCBI36
NG_008408.1:g.42656C>G , LRG_273:g.42656C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.994-99C>G ENSP00000502019.1:n.994-99C>G
ENST00000373477.9:c.1141-99C>G MANE Select ENSP00000362576.4:n.1141-99C>G
ENST00000674629.1:c.*689-99C>G ENSP00000502470.1:n.*689-99C>G
ENST00000674654.1:c.*1101-99C>G ENSP00000501729.1:n.*1101-99C>G
ENST00000675785.1:c.994-99C>G ENSP00000502019.1:n.994-99C>G
ENST00000676297.1:c.*1315-99C>G ENSP00000501596.1:n.*1315-99C>G
ENST00000373477.8:c.1141-99C>G ENSP00000362576.4:n.1141-99C>G
ENST00000469100.5:n.1057-99C>G
ENST00000478828.1:n.608-99C>G
ENST00000487404.5:n.1451-99C>G
ENST00000490826.1:n.335C>G
ENST00000616261.1:c.1140-99C>G ENSP00000484192.1:n.1140-99C>G
NM_003680.3:c.1141-99C>G , LRG_273t1:c.1141-99C>G NP_003671.1:n.1141-99C>G
XM_011542347.1:c.511-99C>G XP_011540649.1:n.511-99C>G
XM_011542348.1:c.511-99C>G XP_011540650.1:n.511-99C>G
XM_011542347.2:c.511-99C>G XP_011540649.1:n.511-99C>G
XM_017002651.2:c.511-99C>G XP_016858140.1:n.511-99C>G
NM_003680.4:c.1141-99C>G MANE Select NP_003671.1:n.1141-99C>G